Analysis of Comments and Implementation of the NIH Public Access Policy, 7603-7614 [E9-3442]
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Federal Register / Vol. 74, No. 31 / Wednesday, February 18, 2009 / Notices
ESTIMATED ANNUALIZED BURDEN TABLE—Continued
Type of respondent
Number of
respondents
Form name
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Trainers of the Revised BodyWorks
program.
Coalition leaders, members, and site
coordinators.
Total Hours ................................
204
204
1
10
30/60
3/60
102
102
63
1
30/60
32
Adolescent Post test Questionnaire
Facilitator Feedback Forms (10
forms).
Coalition Pre test Survey .................
50
22
1
10
30/60
5/60
25
18
86
1
20/60
29
Coalition Post test Survey ................
Adolescent Revised BodyWorks program comparison group participant.
Adolescent Post test Questionnaire
Adolescent
Session
Evaluation
Forms (10 forms).
Adolescent Pre test Questionnaire ..
72
1
30/60
36
...........................................................
........................
........................
........................
755
Dated: February 10, 2009.
Seleda Perryman,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. E9–3439 Filed 2–17–09; 8:45 am]
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DEPARTMENT OF HEALTH AND
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National Institutes of Health
Analysis of Comments and
Implementation of the NIH Public
Access Policy
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
Background
The National Institutes of Health
(NIH) Public Access Policy requires
investigators funded by the NIH to
submit, or have submitted for them, an
electronic version of their final, peerreviewed manuscripts upon acceptance
for publication to the National Library
of Medicine’s digital archive, PubMed
Central, to be posted publicly within 12
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months after the official date of
publication. Congress required the NIH
to implement this funding limitation in
Division G, Title II, Section 218 of the
Consolidated Appropriations Act of
2008 (‘‘Section 218’’). The Policy is
intended to advance science, provide
public access to the published results of
NIH-funded research, and improve
human health.
The current Public Access Policy is
the culmination of years of effort and
community interaction. Prior to passage
of Section 218, the NIH undertook
extraordinary public outreach
concerning the issue of public access to
the published results of NIH-funded
research. These outreach efforts
included a review of over six thousand
public comments and the establishment
of an independent advisory group to
review NIH’s implementation of a
voluntary Public Access Policy.
Additionally, as part of the process to
implement Section 218 in a transparent
and participatory manner, the NIH
formally sought public input through an
open meeting and a Request for
Information (RFI) seeking public
comment. This open meeting occurred
on March 20, 2008, and was designed to
ensure that a discussion of stakeholder
issues could occur. The feedback from
the open meeting helped define
questions for an RFI, which was
published on the NIH Web site on
March 28, 2008 and in the Federal
Register on March 31, 2008 (73 FR
16881–16895). The RFI was designed to
seek input on the NIH Public Access
Policy, as it was revised to incorporate
Section 218, and the responses to
frequently asked questions (FAQs)
concerning it. The RFI was open for
sixty days following publication in the
Federal Register, from March 28 to May
31, 2008.
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administrators, and others in the
comments submitted. Throughout the
In response to the open meeting and
RFI, the NIH received 613 unduplicated course of its analysis, the NIH
comments from a broad cross-section of undertook various efforts to respond to
concerns as it identified them. The
the public, including NIH-funded
agency aimed these actions to clarify the
investigators, members of the general
Public Access Policy and to facilitate
public, patient advocates, professional
compliance with Section 218. In May,
organizations, and publishers. This
July, and September of 2008, NIH
report summarizes these comments.
updated the Public Access Web site to
Most comments offered broad support
clarify the applicability, goals and
for the policy as written. Many
anticipated impact of the policy, the
comments requested a reduction in the
available methods to submit papers, and
delay period before papers can be made
planned methods to document
publicly available on PubMed Central.
compliance. In June 2008, NIH updated
In some cases, commenters expressed
the NIH Manuscript Submission System
concern about the Policy, others asked
(NIHMS), the online mechanism for
for clarification, and still others
submission of manuscripts to PubMed
suggested alternatives to NIH’s
Central (PMC), to allow Program
implementation. These questions and
Directors/Principal Investigators (PDs/
concerns fall into several broad
PIs) to delegate all aspects of submission
categories:
tasks to authors, and to allow publishers
• The potential administrative burden who submit manuscripts to the NIHMS
on Program Directors/Principal
on behalf of authors to exert greater
Investigators and awardee institutions.
control over manuscript delay periods.
• The details of implementing the
In August, the National Library of
Policy, including applicability, cost
Medicine issued a new Web tool to help
reimbursement, compliance monitoring the scientific community obtain
and enforcement, and publisher support PubMed Central Identifiers in bulk. In
of the Policy.
September 2008, NIH issued a Guide
• Associated issues, such as
Notice (NOT–OD–08–119 at https://
submission procedures, tracking
grants.nih.gov/grants/guide/notice-files/
submitted papers, version of the paper
NOT-OD-08-119.html) reminding
submitted, and managing and protecting awardees about the compliance process
copyrights.
and providing details concerning NIH’s
• The accordance of the Policy
monitoring plan for fiscal year 2008.
Implementation with copyright law and
These efforts appear to be working.
the Administrative Procedures Act.
The NIH estimates approximately
• Questions about Policy impact,
80,000 papers arise from NIH funds
such as financial impacts on publishers
each year, and this total serves as the
and NIH.
target for the Public Access Policy.
The NIH also received comments
During the voluntary policy, from May
describing implementation efforts by
2005 to December 2007, the NIH was
numerous awardee institutions and
able to collect a total of 19 percent of
publishers. In some cases, libraries took targeted papers, from all sources. Under
the lead on educating their faculty and
the first five months of the Section 218
supporting them in interpreting
requirement (April to August 2008), this
publishing agreements and submitting
rate jumped to an estimated 56 percent
manuscripts to NIH. In other cases,
of papers per month. While NIH expects
offices of sponsored research provided
to post all of the estimated 56 percent
guidance on the NIH Public Access
of these NIH papers, most of them will
Policy disseminated to their faculty
not be publicly available until 2009.
community via the Web, memos,
These first few months show the
seminars, and video casts. Still other
promise of a Public Access Policy
institutions described collaborations
requirement, its implementation, and
the active support from the academic
between libraries, offices of sponsored
and publishing communities. However,
research, university counsels, and
work still remains as over 40 percent of
technology transfer offices. Several
applicable papers per month remain
universities and private groups
unsubmitted.
described the development of new
Implementation and process
policies on scholarly communications
and new publishing forms and addenda refinement will be continuing in the
coming months. The NIH has
that their faculty could use to ensure
established voluntary partnerships with
compliance with the Policy.
many publishers to facilitate deposit of
NIH Response
manuscripts and final published papers
and expects these partnerships to
The NIH carefully considered the
continue to expand and the percentage
views expressed by publishers, patient
of submitted papers to grow. The NIH
advocates, scientists, university
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Overview of Feedback
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will also continue to engage the
community as we proceed to implement
the Policy in the most efficient and
effective manner possible.
Policy Overview
The NIH Public Access Policy,
announced in January 2008, ensures
that the public has access to the
published results of NIH-funded
research. See https://grants.nih.gov/
grants/guide/notice-files/NOT-OD-08033.html. It requires scientists to submit
final peer-reviewed journal manuscripts
that arise from NIH funds to the digital
archive PubMed Central upon
acceptance for publication. To help
advance science and improve human
health, the Policy requires that these
papers be accessible to the public on
PubMed Central no later than 12 months
after publication.
This Policy implements the
Consolidated Appropriations Act of
2008, which directed the NIH to require
investigators funded by the NIH to
submit, or have submitted for them, an
electronic version of their final, peerreviewed manuscripts upon acceptance
for publication to the National Library
of Medicine’s digital archive, PubMed
Central (PMC), to be posted publicly
within 12 months after the official date
of publication. The Policy builds upon
the experience with NIH’s voluntary
Public Access Policy, which was
published in 2005 and has three aims:
1. ARCHIVE. A central collection of
NIH-funded research publications
preserves vital published research
findings for years to come.
2. ADVANCE. The archive is an
information resource for scientists to
research publications and for NIH to
manage better its entire research
investment.
3. ACCESS. The archive makes
available to the public research
publications resulting from NIH-funded
research.
Policy History
The original, voluntary Public Access
Policy, implemented May 2005 (NOT–
OD–05–022, available at https://
grants.nih.gov/grants/guide/notice-files/
NOT-OD-05-022.html), encouraged but
did not require investigators receiving
NIH funding to deposit their peerreviewed manuscripts into PubMed
Central. It was shaped, in large part,
through discussion with the extramural
community.
The NIH began public discussions on
this topic with three town hall style
meetings in 2004. From this feedback,
the NIH developed a proposal for a
voluntary public access policy that
would make final peer-reviewed
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manuscripts publicly available on
PubMed Central within 6 months of
publication. The NIH issued the
proposed NIH Public Access Policy for
comment in September 2004 (see https://
grants.nih.gov/grants/guide/notice-files/
NOT-OD-04-064.html or https://
a257.g.akamaitech.net/7/257/2422/
06jun20041800/edocket.access.gpo.gov/
2004/04-21097.htm). In response to its
request for input on the proposed
policy, NIH received over 6,200
comments from interested parties,
including grantees, publishers and trade
organizations. After carefully
considering all the comments received,
the NIH published a final policy, NOT–
OD–05–022, on February 3, 2005 (also
published at 70 FR 6891). Though 66
percent of comments favored a sixmonth delay period, the NIH
implemented a voluntary Public Access
policy with a 12-month delay period out
of deference to concerns from some
members of the publishing community.
Implementation of this voluntary
policy was marked by continued
engagement with multiple stakeholders
in order to facilitate participation. The
NIH staff met dozens of times and
exchanged hundreds of letters with
patient advocacy groups, awardee
institutions and their representatives,
publishers, and scientific societies
regarding the Policy. (For a breakdown
of meetings and correspondence, see
slide 12 of NIH Director Elias
Zerhouni’s presentation at the March
20, 2008, open meeting at https://
publicaccess.nih.gov/comments/
Overview_Context.pdf.) In collaboration
with publishers, investigators, grantees,
and others, the NIH established systems
to make it easy for scientists to deposit
their manuscripts directly and for
interested publishers to deposit
manuscripts on scientists’ behalf. For
example, the NIH Manuscript
Submission System (NIHMS), a Web
service built to support the Policy,
allows publishers to submit manuscripts
on behalf of authors in bulk. The NIH
also developed new forms of PubMed
Central Journal agreements in
collaboration with publishers, which
enable publishers to submit final,
published articles to PubMed Central
from NIH-funded authors, only and/or
from authors who pay open access fees
to the journals.
Thus, for almost three years, the NIH
asked the scientists it supports to
deposit their NIH-funded scientific
manuscripts in an NIH online system
that would make them accessible to the
public, freely and in perpetuity. But the
compliance rate under the voluntary
system demonstrated that it would not
achieve the goals of the Public Access
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Policy. In December 2007, the
Consolidated Appropriations Act of
2008 was signed into law, directing the
NIH to require submission of
manuscripts.
Implementing the Consolidated
Appropriations Act of 2008
The Consolidated Appropriations Act
of 2008 (Pub. L. 110–161), at Division G,
Title II, Section 218, directs the NIH as
follows: The Director of the National
Institutes of Health shall require that all
investigators funded by the NIH submit
or have submitted for them to the
National Library of Medicine’s PubMed
Central an electronic version of their
final, peer-reviewed manuscripts upon
acceptance for publication, to be made
publicly available no later than 12
months after the official date of
publication: Provided, that the NIH
shall implement the public access
policy in a manner consistent with
copyright law.
On January 11, 2008, NIH issued the
Public Access Policy implementing this
clear and unambiguous new statute. As
described in the NIH Guide for Grants
and Contracts (NOT–OD–08–033,
available at https://grants.nih.gov/grants/
guide/notice-files/NOT–OD–08–
033.html), the Policy restates the statute
and offers the following specifics:
1. The NIH Public Access Policy
applies to all peer-reviewed articles that
arise, in whole or in part, from direct
costs 1 funded by NIH, or from NIH staff,
that are accepted for publication on or
after April 7, 2008.
2. Institutions and investigators are
responsible for ensuring that any
publishing or copyright agreements
concerning submitted articles fully
comply with this Policy.
3. PubMed Central (PMC) is the NIH
digital archive of full-text, peerreviewed journal articles. Its content is
publicly accessible and integrated with
other databases (see: https://
www.pubmedcentral.nih.gov/).
4. The final, peer-reviewed
manuscript includes all graphics and
supplemental materials that are
associated with the article.
5. Beginning May 25, 2008, anyone
submitting an application, proposal, or
progress report to the NIH must include
the PMC or NIH Manuscript Submission
reference number when citing
applicable articles that arise from their
NIH-funded research. This policy
includes applications submitted to the
NIH for the May 25, 2008 due date and
subsequent due dates.
1 ‘‘Directly’’ funded means costs that can be
specifically identified with a particular project or
activity. See NIH Grants Policy Statement, Rev. 12/
2003.
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7605
Compliance
Compliance with this Policy is a
statutory requirement and a term and
condition of the grant award and
cooperative agreement, in accordance
with the NIH Grants Policy Statement.
For contracts, the NIH includes this
requirement in all R&D solicitations and
awards under Section H, Special
Contract Requirements, in accordance
with the Uniform Contract Format.
In addition to announcing the Policy,
the NIH established a Web site and
posted responses to frequently asked
questions (FAQs) that provide authors,
their institutions, and their publishers
with guidance on the implementation of
the policy.
As part of the process to implement
Section 218 in a transparent and
participatory manner, the NIH formally
sought public input through an open
meeting and a Request for Information
seeking public comment. The open
meeting occurred on March 20, 2008
(NOT–OD–08–057), and was designed
to ensure that discussion of stakeholder
issues could occur. The feedback from
the open meeting helped define
questions for a Request for Information
(RFI), conducted from March 28 to May
31 (NOT–OD–08–060). This report
summarizes comments received at the
meeting and in response to the RFI.
Open Meeting
The purpose of the Thursday, March
20, 2008, meeting was to seek comment
from the public on implementation of
the NIH Public Access Policy. The
meeting was open to all, including NIHfunded researchers, representatives of
universities and other NIH grantee
organizations, publishers (including
commercial organizations, professional
societies, and journal editors), patients
and public health advocates, and
members of the general public. The NIH
desired broad participation and
commentary.
In particular, the NIH was interested
in input concerning the Public Access
Policy and the effectiveness of the
policy’s implementation. Individuals,
groups, and organizations were also
invited to submit written pre-meeting
comments on the NIH Policy.
The NIH made every effort to make
the meeting and pre-meeting comments
open and transparent. Comments were
made public as they were received. The
meeting was video cast, and everyone
who wished to speak was able to. All
meeting materials, including the Guide
Notice, Federal Register Notice, video
cast, transcript, and comments are
available at https://publicaccess.nih.gov/
open_meeting_march_2008.htm.
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Comments posted on this site are
recorded as submitted and, in some
cases, include duplicates.
Request for Information (RFI)
The feedback from the open meeting
helped define questions for a Request
for Information (RFI), which was
published on the NIH Web site on
March 28, 2008, and in the Federal
Register on March 31, 2008 (73 FR
1681–1695) (see NOT–OD–08–060). The
NIH sought information from the public,
including all stakeholders, about the
new NIH Public Access Policy and the
frequently asked questions developed to
assist investigators to implement it.
Among other issues, the NIH
particularly sought information about
the following questions:
• Do you have recommendations for
alternative implementation approaches
to those already reflected in the NIH
Public Access Policy?
• In light of the change in law that
makes NIH’s public access policy
mandatory, do you have
recommendations for monitoring and
ensuring compliance with the NIH
Public Access Policy?
• In addition to the information
already posted on the NIH Web site,
what additional information, training or
communications related to the NIH
Public Access Policy would be helpful
to you?
Individuals, groups, and organizations
interested in responding were invited to
do so via a Web site that would record
their responses for each question and
make those responses publicly
available. All comments received via the
Web and e-mail related to the Public
Access Policy RFI is now available at
https://publicaccess.nih.gov/
comments.htm.
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Methodology for Analysis
Consolidating and Categorizing
Comments
Comments were posted as they were
collected, and commenters had the
opportunity to respond to other
comments. This was a deliberate effort
on the part of NIH to encourage dialogue
among stakeholders and to provide a
more synthesized set of ideas for
analysis. Individuals and organizations
were allowed to submit multiple
comments, and all comments were
treated equally, regardless of the source.
Although the NIH requested input on
several open-ended questions at the
meeting and in the RFI, commenters did
not restrict themselves to input on these
questions and offered a variety of
opinions on other topics, either in
addition to responding to the questions
or in lieu of responding to them.
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Combined, the open meeting and RFI
yielded 613 unduplicated comments.
The comments include materials
entered through the online comment
service, transcriptions of in-person
statements offered at the March 20 Open
Meeting, and e-mails received at the
Public Access comments mail box.
Duplicates were identified by finding
multiple comments from the same
individual that contained identical
content. Comments that were entirely
off-topic (e.g., SPAM, selling products)
were considered nonresponsive and
thus not counted. If an individual
submitted multiple responses and each
submission contained new content, they
were not marked as duplicates and were
separately counted and analyzed. In
addition, if the same comment or
information (e.g., a form letter) was
received from two or more individuals
those comments were counted
separately and not marked as
duplicates.
All unduplicated comments
underwent an initial review to identify
the topic(s) addressed and to gain a
sense of the relative number of
commenters who addressed each topic.
This initial analysis helped to identify
major themes for inclusion in this
report.
The 613 unduplicated comments
covered by this report, combining
comments from both the open meeting
and the RFI, and including PDF
comments converted to text using
optical character recognition, became
available in a single file at https://
publicaccess.nih.gov/comments.htm in
October 2008. We invite our
stakeholders to use these resources to
conduct independent analyses of these
data.
The public comments were largely
supportive of the Policy. Comments
clustered around several broad themes.
We describe them below, followed by
NIH’s analysis and response where
appropriate.
1. Need for the Policy
The most common theme among
comments, expressed in a large majority
of all comments, was support for the
Policy as written. When reasons for
support were offered, the most common
were as follows: (1) The perceived
benefit to patients and their families, (2)
the belief that the American public has
a right to access papers arising from NIH
funds, and (3) the expected potential of
the policy to advance scientific
discovery. A small minority of
comments expressed general
disagreement with the Policy and/or felt
that increasing access to papers arising
from NIH funds was unnecessary.
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2. The Length of the Delay Period
The second largest number of
comments, second only to general
support for the Policy, were comments
advocating reducing the period of time
before papers are made publicly
available on PubMed Central. A large
number of commenters argued for a
shorter maximum delay period—many
suggested 6 months, many no delay
period at all, and a few suggested 3
months. Advocates for reducing the
period of time explained that doing so
would provide greater benefits to the
public and to science. Some further
claimed, and provided examples of
how, shorter delay periods would not
harm publisher interests. A few
commenters suggested that the
maximum delay period should be
greater than 12 months. These
commenters claimed that a longer delay
period was needed to protect journals in
certain disciplines.
The NIH appreciates the concerns of
all commenters concerning the
maximum delay period between journal
publications and posting on PubMed
Central. The Consolidated
Appropriations Act of 2008 specifies the
maximum delay period at 12 months.
Copyright holders may always post
materials with a shorter delay period, at
their discretion.
3. Actions Taken by Institutions to
Support Implementation
Many commenters shared their efforts
to implement and promote the Policy.
Several publishers described their
efforts to support implementation,
either by facilitating submission of
papers on behalf of their authors, or by
offering new guidance and publishing
agreements so that their authors may
understand how to comply with the
Policy.
A number of awardee institutions
offered their implementation strategies
as well. In some cases, libraries were
taking the lead in educating their faculty
and supporting them in interpreting
publishing agreements and submitting
manuscripts to the NIH. In other cases,
offices of sponsored research described
guidance on the NIH Public Access
Policy disseminated to their faculty
community via the Web, memos,
seminars, and video casts. Still other
institutions described collaborations
between libraries, offices of sponsored
research, university counsel, and
technology transfer offices. Several
universities and private groups also
described institutional policies on
scholarly communication and new
publishing forms and addenda that their
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faculty could use to ensure compliance
with the Policy.
The NIH is interested in the role
institutions may play in supporting the
Policy and appreciates the efforts of
these commenters to both support the
policy and share their strategies. In
January 2008, the NIH published an
article outlining key questions
institutions may wish to consider as
they implement the Policy (https://
grants.nih.gov/grants/partners/
0108Nexus.htm#investigator). Based on
the comments submitted, it appears that
the community has developed multiple
approaches to issues described in this
article, but it is too early in the
implementation of the Policy to
determine if some approaches are more
successful than others.
NIH employees publish several
thousand peer-reviewed papers each
year, and the NIH has to support the
Policy as an investigator institution as
well. Our approach to ensure
compliance among our own faculty
involves support from the NIH Library,
a unit of the NIH Office of Research
Services; NIH technology transfer
representatives; and the NIH Office of
Intramural Research. The NIH offers
employees guidance on our Web site, a
publishing agreement addendum,
centralized negotiation of publishing
agreements, help desk support for
manuscript submission and policy
questions, and staff training upon
request. See https://publicaccess.nih.gov/
nih_employee_procedures.htm for more
information.
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4. Administrative Burden for
Institutions and Principal Investigators
Some comments expressed concern
that the Policy would create undue
burdens on authors, investigators, and
institutions. The comments are
described below.
A. Negotiating Publisher Agreements
Some comments suggested the Policy
required authors and individual
investigators to negotiate with
publishers directly. They felt individual
authors lacked the skills or bargaining
power to develop an agreement with a
publisher that met their needs under the
Policy.
Investigators are central to
implementing the Policy and usually are
the initial copyright holder of the
manuscripts that fall under the Policy.
They may need to negotiate the terms of
publishing agreements with publishers
directly. However, the NIH expects that
institutions will support their
investigators in complying with terms
and conditions of award. The NIH
Public Access Policy states ‘‘Institutions
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and investigators are responsible for
ensuring that any publishing or
copyright agreements concerning
submitted articles fully comply with
this Policy.’’ The NIH underscores the
importance of institutional support
throughout the Frequently Asked
Questions (FAQ). For example, FAQ C4
addresses publishing agreements or
publishers that may not support
compliance with the Policy. FAQ C11,
released in May 2008 in response to this
feedback, addresses another aspect of
this concern. In both cases, the NIH
encourages authors and investigators to
work with their institution’s office of
sponsored research.
With regard to particular agreement
terms, individual copyright
arrangements can take many forms, and
authors and their institutions should
continue to manage such arrangements
as they have in the past.
Institutions and investigators may
wish to develop particular copyright
agreement terms in consultation with
their own legal counsel or other
applicable official at their institution, as
appropriate. As an example, the kind of
language that an author or institution
might add to a copyright agreement
includes the following (as described in
FAQ C3):
‘‘Journal acknowledges that Author
retains the right to provide a copy of the
final peer-reviewed manuscript to the
NIH upon acceptance for Journal
publication, for public archiving in
PubMed Central as soon as possible but
no later than 12 months after
publication by Journal.’’
There are many other potential
models, some of which were described
in other comments and are available for
viewing therein.
B. Ability for Investigators to Publish in
the Journal of Their Choice
A few comments expressed concern
that some journals would refuse to
allow manuscripts to be posted to PMC
in accordance with the Policy, and
authors would not be able to publish in
those journals. They claimed this could
occur despite an author’s best efforts to
negotiate with a publisher.
The NIH agrees that author choice of
publication is a very important issue,
but if this situation were to occur, an
author might have to find an alternate
journal. Therefore, the NIH encourages
authors to clearly communicate with
and address these issues before they
may transfer their copyright and
potentially lose their ability to comply
with the Policy. The Public Access
Home page states: ‘‘Before you sign a
publication agreement or similar
copyright transfer agreement, make sure
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7607
that the agreement allows the paper to
be submitted to NIH in accordance with
the Public Access Policy.’’
The NIH has also engaged the
publishing community in order to
minimize copyright concerns when
possible. The NIH has established
voluntary partnerships with many
publishers who agree to facilitate
deposit of manuscripts and final
published papers. The number of papers
submitted via these agreements has
grown since the Public Access Policy
took effect. The NIH issued guidance to
authors to clarify these various
arrangements in July 2008. The
guidance can be found at https://
publicaccess.nih.gov/
submit_process.htm. Whether because
of NIH’s direct efforts, clear
communication from authors and
institutions or because of publisher
support for the Policy, NIH did not
receive comments indicating that
publishers or publishing agreements
have actually prevented authors from
complying with the Policy. To the best
of our knowledge, this concern
currently remains a hypothetical risk
and not a manifest problem.
C. Cost Reimbursement
Some commenters raised the issue of
investigators or awardees needing to pay
potential publishing costs and fees
associated with the Policy (e.g., fees for
posting to PubMed Central, fees to
reduce delay periods). Some
commenters suggested that the NIH
should cover these costs, others
requested clarification concerning costs,
and still others thought the NIH would
offer no financial support to either
institutions or publishers. As such, the
commenters felt that the Policy was an
unfunded mandate that might harm
author or publisher interests, with
junior authors (new investigators and
trainees) being especially vulnerable.
However, several commenters thought
any unrecovered costs associated with
the Policy were worth the benefits, and
one commenter even requested that the
NIH stipulate that costs not be covered.
As with other costs, the NIH will
reimburse publication costs, including
author fees, for grants and contracts on
three conditions: (1) Such costs incurred
are actual, allowable, and reasonable to
advance the objectives of the award; (2)
costs are charged consistently regardless
of the source of support; (3) all other
applicable rules on allowability of costs
are met. Generally, page charges for
publication in professional journals are
allowable if the published paper reports
work supported by the grant and the
charges are levied impartially on all
papers published by the journal,
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whether or not they are submitted by
Government-sponsored authors.
D. Compliance Burden
Some commenters expressed concern
about the time Program Directors/
Principal Investigators (PDs/PIs) and
authors will need to spend to submit
papers. A few commenters said that a
simple submission system was critical
to the success of the policy. Among
those commenting on the potential
burden of the submission process, a
portion said the existing NIH
Manuscript Submission System
(NIHMS) was easy to use, a portion said
it was complex and burdensome, and a
portion were unaware of how it worked.
Some commenters also expressed
concern or offered suggestions related to
the notification and management of
PubMed Central Identifiers (PMCIDs),
which are assigned to papers after they
are submitted and can be used to
demonstrate compliance with policy on
applications, proposals, and reports.
The NIH agrees with the need to have
a simple manuscript submission process
to minimize the time associated with
deposit of manuscripts into PubMed
Central. NIH has worked diligently
since the adoption of the voluntary
Public Access Policy in 2005 to develop
a streamlined and efficient process.
During the voluntary Policy, NIH found
it took authors about 10 minutes to
deposit a paper in the NIH Manuscript
Submission System (NIHMS); the time
decreased for submitters as they began
to submit more papers and gained
experience with the system.
The NIH continues to refine the
NIHMS as necessary. For example,
starting in June 2008, NIH eliminated
the need for PDs/PIs to review each
deposit. Instead, the NIHMS now allows
authors to complete all aspects of
manuscript submission, with the idea
that greater flexibility in delegation will
minimize PD/PI burden. The NIH gives
specific guidance on these submission
processes on its Web site at https://
publicaccess.nih.gov/
submit_process.htm. This guidance also
describes how authors can delegate
some submission tasks to someone in
the author’s organization (e.g., an
assistant or a librarian), or to their
publisher, and how all aspects of
submission can be delegated to a
publisher that participates in PubMed
Central.
The NIH has developed Policy
compliant alternatives to manuscript
deposit that require less author effort.
For example, as described at https://
publicaccess.nih.gov/
submit_process.htm, some publishers
sign agreements with the NIH to submit
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final published articles directly to
PubMed Central without author
involvement. Since the passage of the
2008 Consolidated Appropriations Act,
the number of publishers signing such
agreements has significantly increased.
The NIH has also made changes to the
way it reports PubMed Central reference
numbers (PMCID), and how authors and
delegates can use the NIHMS system.
For example, as described in FAQ C9,
issued May 2008, the PMCID is posted
in PubMed as soon as an article has
been successfully processed by PMC,
which usually occurs around the time of
publication. PMCIDs are listed in the
lower right corner of the Abstract Plus
view of PubMed (https://
www.ncbi.nlm.nih.gov/PubMed/). If the
paper is not yet publicly available on
PMC, PubMed will also list the date the
paper will become available. The NIH
provides other methods of obtaining
PMCIDs (e.g., https://
www.ncbi.nlm.nih.gov/sites/
pmctopmid, created in August 2008), as
do several bibliography management
software packages.
E. Collaborations With Institutional
Repositories
As a way to relieve compliance
burdens on their faculty, a few
institutions requested direct feeds from
their repositories to PubMed Central or
the NIH Manuscript Submission system.
The NIH believes that these are
worthwhile suggestions, but it is
concerned that they raise important
technical and logistical challenges
regarding author approval, copyright
permissions, quality control, and
formats for electronic transfer. The NIH
remains open to closer collaboration
with institutional archives and will
consider this issue as the Policy
matures. National Library of Medicine
representatives met with representatives
from academic communities to discuss
this issue in November 2008.
5. Expanding the Scope of the Public
Access Policy
Some commenters suggested the
Policy be expanded in several ways
from investigators and research funded
by additional or all Federal research
funds to papers published before April
7, 2008, or to the data and unpublished
results associated with an award. A few
comments suggested a specific
alternative approach to expand the
scope of the policy to exempt all works
arising from NIH/Government funds
from copyright protection.
The NIH understands and appreciates
the strongly held views of many
commenters concerning access to works
funded by the NIH and the Government
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generally. The NIH Public Access Policy
implements the Consolidated
Appropriations Act of 2008, Division G,
Title II, Section 218 (Pub. L. 110–161),
a Federal statute that was passed by
Congress and signed by the President of
the United States. This statute is very
specific—it indicates what is to be
submitted and when, and when and
where submissions are made publicly
available.
The NIH’s new Access Policy took
effect a few months after passage of the
law to allow copyright holders to make
arrangements to post directly and in
accordance with copyright law.
Regarding the suggestion that works
funded through the NIH should be
denied copyright protection, we note
that works of Government employees,
including NIH investigators, are not
subject to copyright protection in the
United States (17U.S.C. 105). The works
of Government awardees, however, are
subject to copyright protection.
6. Issues About the Policy and Its
Implementation Requiring Clarification
A number of issues were raised that
resulted in NIH providing clarifications.
A. Compliance Monitoring and
Enforcement
A number of comments suggested that
investigators should include evidence of
compliance with the Policy in
applications, proposals or reports
submitted to the NIH. A few comments
simply asked what is the process for
enforcing compliance.
It is unclear whether the commenters
proposing reference within NIH
applications, proposals, or reports were
endorsing the Policy as implemented, as
it already specifies that investigators
should do so, or were unaware of the
compliance procedure described in the
January 11, 2008 Guide notice. As is
made clear therein, the NIH expects that
investigators citing their NIH-funded
papers subject to the Policy in NIH
applications, proposals, or progress
reports will include the PubMed Central
reference number for each applicable
paper.
The NIH clarified the compliance
reporting process with an update to the
Web site in May 2008 and further
clarified the compliance documentation
and monitoring processes in a Guide
Notice (OD–NOT–08–119 at https://
grants.nih.gov/grants/guide/notice-files/
NOT-OD–08–119.html). FAQ C8, also
part of the May 2008 release, clarifies
that the Policy reporting requirement for
applicants and PDs/PIs only applies to
papers that are authored by them or
arose from their NIH award and fall
under the policy.
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Some commenters also asked about
consequences for PDs/PIs and
institutions if manuscripts are not
submitted as required by the law and
the Policy. Generally, and as specified
in the NIH Guide for Grants and
Contracts, a grantee’s failure to comply
with the terms and conditions of award
may cause the NIH to take one or more
enforcement actions, depending on the
severity and duration of the
noncompliance. The NIH will undertake
any such action in accordance with
applicable statutes, regulations, and
policies. The NIH generally will afford
the grantee an opportunity to correct the
deficiencies before taking enforcement
action unless public health or welfare
concerns require immediate action.
However, even if a grantee is taking
corrective action, the NIH may take
proactive action to protect the Federal
Government’s interests, including
placing special conditions on awards or
precluding the grantee from obtaining
future awards for a specified period, or
may take action designed to prevent
future noncompliance, such as closer
monitoring. See Enforcement Actions in
the NIH Grants Policy Statement (11/
03): https://grants.nih.gov/grants/policy/
nihgps_2003/
NIHGPS_Part8.htm#_Toc54600145.
B. Preventing Copyright Violations on
PMC
The NIH received feedback on the
potential copyright implications of
posting papers to PubMed Central
(PMC), which cluster into two themes.
Some comments asked how the NIH
will prevent inappropriate posting of
materials to PMC without permission of
the copyright holder or posting prior to
expiration of the delay period specified
by the submitter. Other comments,
described below, expressed concern
about the operation of PMC and the
protections it offers copyright holders
against inappropriate use of their works.
The comments about inappropriate
posting primarily focused on
individuals posting content without
copyright permission. The NIH
manuscript submission system is the
only way in which authors may deposit
manuscripts to PMC. That process
requires the author to confirm he or she
has the right or permission for the
specific version submitted to be posted
to PMC after the specific delay period.
Publishers and authors have
occasionally disagreed on the terms of
their publishing agreements. Publishers
have submitted final peer-reviewed
manuscripts on behalf of their authors
requesting a specific delay period, and
in the course of approving the
manuscript for posting, authors have
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selected a shorter delay period. In June
2008, NIH modified the NIH Manuscript
Submission System to allow a publisher
to fix the delay period when they
submit a manuscript on behalf of their
authors. Authors now have to contact
NIH and their publisher if they wish to
change the delay. We expect this more
direct communication will result in
fewer disagreements about delay
periods.
Commenters also asked how NIH
safeguards privately copyrighted
materials on PubMed Central once it is
posted. NIH has eight years of
experience in safeguarding copyrighted
material on the PMC Web site, the host
archive of the Public Access Policy.
There are over 1.5 million full-text
articles on the Web site. PMC has
algorithms to detect inappropriate use,
such as bulk downloading, and sites
responsible for inappropriate use are
warned of the consequences of violating
copyright provisions and blocked from
further access.
C. Applicability of the Policy
Some commenters asked questions or
expressed confusion about the papers to
which the Policy applies. Applicability
was clarified in the May 2008 FAQ B1.
The Policy applies to any manuscript
that:
Is peer-reviewed;
• And, is accepted for publication in
a journal on or after April 7, 2008.
• And, arises from:
• Any direct funding 2 from an NIH
grant or cooperative agreement active in
fiscal year 2008, or;
• Any direct funding from an NIH
contract signed on or after April 7, 2008,
or;
• Any direct funding from the NIH
Intramural Research Program, or;
• An NIH employee.
Consistent with the NIH’s longstanding interest in developing a full
and complete database, however,
authors may also submit final peerreviewed manuscripts accepted before
April 7, 2008, that arise from NIH funds,
if they have appropriate copyright
permission or authority.
D. Version Control
The NIH received comments with
questions or concerns about the version
of the paper posted to PMC. Some
commenters suggested that only final,
published versions of articles should be
posted as they felt final peer-reviewed
manuscripts may contain scientific
errors corrected during the copy-editing
2 ‘‘Directly’’ funded means costs that can be
specifically identified with a particular project or
activity. See NIH Grants Policy Statement, Rev. 12/
2003.
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process. A few commenters expressed
concern that the formatting processes
that are part of PubMed Central may
change the meaning of the paper.
The NIH has been posting final peerreviewed manuscripts on PMC for years
and found them to offer the same
scientific information as the final
published article. The NIH obtains the
permission of the author before each
author manuscript is posted to PMC. We
ask authors to review the specific
document to be posted, and allow them
to correct any scientific issues during
the approval process and afterwards. To
date, we are unaware of uncorrected
errors in PubMed Central.
In response to questions about the
version of a paper that may be posted
on PMC, the NIH issued FAQ D6 in May
2008. It explains that the NIH Public
Access Policy is based on a law
(Division G, Title II, Section 218 of Pub.
L. 110–161) that requires investigators
to submit ‘‘their final, peer-reviewed
manuscripts’’ to PubMed Central. The
NIH will accept the final published
article in lieu of the final peer-reviewed
manuscript, provided that the submitter
has the right to submit this version.
Some journals post final published
articles directly to PMC. See https://
publicaccess.nih.gov/
submit_process_journals.htm for more
information.
Papers need to be converted into the
PMC Archival format in order to be
posted. This process does not change
the meaning or the content of the paper.
However, it does further the goals of the
Public Access Policy and is a
fundamental feature of the PMC
database. Once posted to PubMed
Central, results of NIH funded research
become more prominent, integrated, and
accessible, making it easier for all
scientists to pursue NIH’s research
priority areas competitively. PubMed
Central materials are integrated with
large NIH research databases such as
Genbank and PubChem, which helps
accelerate scientific discovery. Finally,
the Policy allows the NIH to monitor,
mine, and develop its portfolio of
taxpayer-funded research more
effectively and archive its results in
perpetuity.
The NIH should provide guidance on
copyright issues.
Some commenters requested explicit
guidance on copyright issues. The NIH
provides an example in FAQ C3 (https://
publicaccess.nih.gov/FAQ.htm#c3),
which states that ‘‘* * * Individual
copyright arrangements can take many
forms, and authors and their institutions
should continue to manage such
arrangements as they have in the past.’’
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Institutions and investigators may
wish to develop particular copyright
agreement terms in consultation with
their own legal counsel or other
applicable official at their institution, as
appropriate. As an example, the kind of
language that an author or institution
might add to a copyright agreement
includes the following:
‘‘Journal acknowledges that Author
retains the right to provide a copy of the
final peer-reviewed manuscript to the
NIH upon acceptance for Journal
publication, for public archiving in
PubMed Central as soon as possible but
no later than 12 months after
publication by Journal.’’
7. Requests for Additional Information
About the Policy and Implementation
Procedures.
A. NIH Should Disseminate Information
About Publisher Support of the Policy
Some commenters asked for a list of
publishers that allow their authors to
comply with the policy. NIH has
developed and maintains two lists of
publishers and journals. Hundreds of
journals make the final published
version of every NIH-funded article
publicly available in PubMed Central
within 12 months of publication
without author involvement. See https://
publicaccess.nih.gov/
submit_process_journals.htm for a list of
these journals. Some publishers will
deposit an individual final published
article in PubMed Central upon author
request, and generally for a fee. See the
list of publishers at https://
publicaccess.nih.gov/
select_deposit_publishers.htm. All other
publisher policies and procedures
require active author involvement to
finalize submission, as described in
Methods C and D of the Policy Web site
(see https://publicaccess.nih.gov/
submit_process.htm).
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B. Frequently Asked Questions
Some commenters specifically
highlighted the Frequently Asked
Questions as a helpful resource. A few
mentioned the Public Access Policy
Web site in its entirety as helpful. The
NIH also offers additional resources to
support training efforts, including
complete slide presentations that may
be downloaded and adopted for
stakeholder use. These are available at
https://publicaccess.nih.gov/
communications.htm.
8. Implementation Alternatives
A. Administrative Procedure Act
Some commenters felt the
implementation of the Public Access
Policy was in violation of the
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Administrative Procedure Act. They
claimed the NIH should not have
implemented the Policy without going
through a notice and comment
rulemaking and that the January 11
Guide Notice (https://grants.nih.gov/
grants/guide/notice-files/NOT-OD–08–
033.html) was issued inappropriately.
The NIH believes the initiation of
notice and comment rulemaking to
implement the new statute is
unwarranted and contrary to the
interests of science and the public
health. The mandatory access
requirement now adopted in NIH Public
Access Policy derives from Public Law
110–161, § 218, a Federal statute that
was passed by Congress and signed by
the President of the United States. This
statutory provision is a clear and
unambiguous directive to the NIH
Director to require NIH grantees to
provide their manuscripts to PubMed
Central after the date of publication.
Where, as is true in this case, a statute
clearly directs an agency to execute a
congressional objective, and Congress
has not directed the agency to
promulgate implementing regulations,
an agency’s interpretation or statement
of policy or procedure regarding the
statute does not trigger a requirement for
notice and comment rulemaking. 5
U.S.C. 553(b)(3)(A); see also Shalala v.
Guernsey Mem. Hosp., 514 U.S. 87, 99
(1995); American Mining Congress v.
Mine Safety & Health Admin., 995 F.2d
1106, 1112 (D.C. Cir. 1993). Further, the
only significant difference between the
new law and the NIH’s former voluntary
public access policy is implementation
of the legal directive to require
provision of the manuscripts; there is no
‘‘gap’’ left by Congress that would
require a rule to implement the statute.
See Chevron, U.S.A., Inc. v. NRDC, Inc.,
467 U.S. 837, 843–44 (1984). The
mechanics of implementing the former
policy were widely understood as
described in published agency policy
and in widely accessible Internet
resources maintained by the NIH.
Furthermore, the mechanics of
implementing the new statute are
substantially the same as, and consistent
with, the NIH’s earlier policy
implementation. Agency
implementation of a plainly worded
Congressional mandate—particularly
where consistent with established
agency policy—does not require a
rulemaking proceeding. See, e.g., Gray
Panthers Advocacy Cmte. v. Sullivan,
936 F.2d 1284, 1291 (D.C. Cir. 1991). To
the extent the NIH has offered, and
continues to offer, interpretative policy
guidance or procedural assistance with
regard to the new law, such guidance is
not of free-standing legal effect but
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rather is intended to assist grantees to
comply with their statutory obligations.
See American Mining Congress, 995
F.2d at 1112. The impact of the
mandatory submission requirement
arises from the statute, and rulemaking
is not necessary to implement this
statutory requirement.
B. America Competes Act
Some commenters suggested the
America Competes Act as an alternative
to the NIH’s implementation. Relying on
dissemination of reports and abstracts as
described in the America Competes Act
is not consistent with the Consolidated
Appropriations Act of 2008.
C. A ‘‘Dark Archive’’ or Linking to
Publisher or Other Web Sites
A few comments suggested that
awardees should submit manuscripts to
the NIH for internal NIH reporting and
portfolio management, and public
access could be provided by links to
freely available materials on publisher
sites. Some comments suggested that the
NIH only provide public access via
publisher sites, and not maintain an
internal archive at all. Many comments
explicitly repudiated these ‘‘dark
archive’’ or linking approaches and
argued that the policy should require
deposit to PubMed Central. One
comment suggested that the Public
Access Policy mandate deposit to
institutional archives (i.e., those
maintained by universities), and that
these repositories could submit papers
to PubMed Central.
The Consolidated Appropriations Act
of 2008 explicitly states that papers
should be submitted to and made
publicly available on PubMed Central
and the NIH must follow this law.
PubMed Central (PMC) is the NIH
National Library of Medicine’s (NLM)
digital repository of full-text, peerreviewed biomedical, behavioral, and
clinical research journals. NLM and its
predecessor organizations have been
archiving the biomedical literature for
over 150 years and are experienced in
maintaining a stable archive of scientific
information. PMC is currently used by
approximately 400,000 users per day.
There are several critical advantages
to the scientific community for making
papers publicly available on PMC. Once
posted to PMC, results of NIH-funded
research become more prominent,
integrated, and accessible, making it
easier for all scientists to pursue NIH’s
research priority areas competitively.
PMC materials are integrated with large
NIH research databases such as Genbank
and PubChem, which helps accelerate
scientific discovery. Clinicians, patients,
educators, and students can better reap
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the benefits of papers arising from NIH
funding by accessing them on PMC at
no charge. Finally, the Policy allows
NIH to monitor, mine, and develop its
portfolio of taxpayer-funded research
more effectively, and archive its results
in perpetuity.
The Public Access Policy does not
state that PMC will be the sole
repository for these manuscripts and
publications. The NIH has always
pointed to journal and publisher sites
from PMC and PubMed and will
continue to do so. See https://
www.ncbi.nlm.nih.gov/projects/linkout/
for more information. Others may also
post and/or archive papers arising from
NIH funds at other locations, subject to
permission from copyright holders, as
appropriate.
9. Copyright Issues
A. Consistency With Copyright Law
The Consolidated Appropriations Act
of 2008 requires that the NIH implement
the policy consistent with copyright
law. Some commenters suggested that
that might not be possible.
The NIH disagrees with commenters’
suggestions that it will be difficult to
implement the new statute in a manner
that is consistent with copyright law. To
the contrary, the effect of the new
statute is merely that an author of a
work that was funded by grants from the
NIH must retain, from the entire
‘‘bundle of rights’’ 3 inherent in a
copyrightable work, a right to provide
the author’s manuscript to PubMed
Central for display on its Web site. The
author (or his or her employer) could,
for instance, address this point in the
agreement with the publisher by a
simple statement that reserves, on
behalf of the assignor, the right to
provide the manuscript to PubMed
Central for display. Such a reservation
of rights by the author is clearly
consistent with copyright law and the
Consolidated Appropriations Act of
2008.4
3 See
17 U.S.C. 106.
in a manuscript vests initially with
the author and remains with the author unless the
rights are expressly assigned. 17 U.S.C. 201(a). Of
course, the author may be hired to write the
manuscript or may otherwise enter into an
arrangement that assigns the rights to an employer,
making the employer the author for purposes of the
Copyright Act. 17 U.S.C. 201(b). Nevertheless, the
author owns all of the rights in the manuscript, and
a potential publisher owns no rights, unless and
until they are conveyed by the author to the
publisher. A publisher that subsequently obtains
copyright to the work can continue to hold and
enforce all of the rights transferred by the author,
subject to the principles of the fair use doctrine, as
are all copyrights. PubMed Central includes many
copyrighted works, and public use of a work on
PubMed Central is constrained by copyright,
including the principles of fair use, just as it would
U.S. Copyright law anticipates the
transfer of ownership rights in a
copyright by agreement among parties
or by operation of law (17 U.S.C.
201(d)). Publishers do not own any
portion of a copyright in a work that is
not transferred to them by the author,
or, if it is a work for hire, under an
employment agreement with the
employing institution. Similarly, the
Federal Government, through OMB
Circular A–110, grants federally funded
institutions the right to retain intangible
property (including copyright) as part of
the terms and conditions of a Federal
grant. Congress could, if it wished,
require grantees to assign all rights to
intangible property to the Federal
funding agency, as indeed was the case
for patent rights prior to the Bayh-Dole
Act of 1980. However, in recognition of
the public interest in having biomedical
scientific publications widely
accessible, Congress has required only
that NIH-funded authors reserve the
right to post works on PubMed Central.
As one among dozens of conditions
imposed on a grantee by Congress in
return for taxpayer support of the
grantee’s work, the reservation of this
small sliver of the entire bundle of
rights inherent in the work is
completely consistent with U.S.
Copyright law.
B. Value of Publisher-Held Copyrights if
Other Aspects of Copyright Are
Retained by Authors
A few comments indicated concern
that posting the final peer-reviewed
manuscript to PubMed Central
undermines the value of all other
aspects of copyright that a Publisher
may have obtained under the Policy.
As described above, it is acceptable
from a copyright perspective for
investigators to ensure their papers can
be posted to PubMed Central. However,
the NIH Public Access Policy applies to
awardees, not publishers. The NIH
implemented the Public Access Policy
prospectively to ensure that publishers
have the ability to refuse to publish any
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be if a member of the public viewed the publication
in a library, for example. Further, the public is
alerted that the works they are viewing may be
subject to copyright, with the following statement:
‘‘This site also contains resources such as PubMed
Central, Bookshelf, OMIM, and PubChem which
incorporate material contributed or licensed by
individuals, companies, or organizations that may
be protected by U.S. and foreign copyright laws. All
persons reproducing, redistributing, or making
commercial use of this information are expected to
adhere to the terms and conditions asserted by the
copyright holder. Transmission or reproduction of
protected items beyond that allowed by fair use
(https://www.copyright.gov/fls/fl102.html) as defined
in the copyright laws requires the written
permission of the copyright owners.’’ [https://
www.ncbi.nlm.nih.gov/About/disclaimer.html]
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paper they wish, for any reason they
wish, including not obtaining all the
rights they may prefer from authors of
papers arising from NIH funds. The 12month delay period and the ability of
NIH awardees to cover publicationrelated costs from their awards are
important aspects of the Policy created
specifically to address concerns of some
publishers and ensure their interests are
protected.
These comments concerning loss of
value of the copyrighted work were not
supported by data and run contrary to
NIH’s experience. The voluntary
support of hundreds of journals to
collect papers under the Policy is,
perhaps, a reflection of publisher
protections in the Public Access Policy.
A significant number of journals
support their authors by volunteering to
submit manuscripts, and many more go
beyond the policy by submitting final
published articles. Hundreds even
deposit final published articles that do
not arise from NIH funds. Many of these
journals also permit their papers to be
posted to PubMed Central before the 12month maximum delay period. The NIH
appreciates the efforts of all these
journals to support the Policy.
C. Section 201(E) of the Copyright Act
One comment raised a concern that
Section 201(e) of the Copyright Act
prohibits a requirement for NIH
awardees to retain a right to deposit in
PMC. Section 201(e) of the Copyright
Act states that when an individual
author’s ownership of a copyright has
not previously been transferred
voluntarily by that individual author, no
action by any governmental body
purporting to seize copyright shall take
effect.
Section 201(e) does not apply to the
PMC situation for many reasons. First,
the works at issue here are for the most
part works in which the author has
already expressly agreed how copyright
will be handled through the
employment agreement with their
employing institution (see 201(b) works
made for hire). Second, the employing
institution will have previously
accepted, as a term and condition of the
grant, the obligation to submit a work
created under the grant to PMC. Third,
Congress did not require an involuntary
transfer of rights, or otherwise ‘‘seize’’
rights. Rather, it required submission of
the manuscript to PMC. One way of
complying with this requirement would
be for the author to retain the right to
post, rather than transfer that right to a
third party. Such retention by the author
does not constitute a seizure or
involuntary transfer of rights.
Copyrighted material on PMC remains
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fully subject to copyright, and copyright
owners may fully enforce their rights.
Fourth, to the extent that the PMC
requirement can be read as a
Government-retained interest, Congress
often requires funding agencies to retain
certain rights in the public interest in
tangible and intangible property first
produced with public funds. To read the
patent or copyright laws as preventing
such action would overturn many longstanding provisions of OMB Circular A–
110 as well as the Federal Acquisition
Regulation (F.A.R.) (e.g., rights in data
first produced in its procurement
contracts, rights in inventions, rights in
computer software).
not conflict with the normal
exploitation of the work. But the
deposition requirement makes no
limitation on the exclusive rights
attached to the work. It merely requires,
as a reasonable and mutually agreed
condition of the grant award, that the
author or its institution reserves the
right to display the author’s manuscript
on PMC. If the PMC deposition
requirement violates TRIPS, then any
Government procurement contract that
secures rights to works made under the
contract would also violate TRIPS. No
compelling argument for that
proposition has been presented to the
NIH.
D. International Copyright Issues
A few comments suggested that
copyright concerns stem from making
materials available on the Internet, and
therefore internationally available. The
NIH appreciates that the scientific
community is truly global and
interchange among scientists worldwide
is essential for professional and
scientific advancement. The Policy
applies to all NIH-funded investigators,
including those in foreign countries.
The PMC archive is available through
the Internet, and therefore globally.
Copyrights on works displayed in PMC
are fully enforceable by the copyright
owners in the U.S. and abroad. The NIH
notes that many publishers post
materials to their Web site, which also
makes them globally available.
One comment raised specific
concerns about the Berne Convention
and the World Trade Organization
(WTO) TRIPS provision. The Berne
Convention’s provisions require that
member countries provide protection for
literary and artistic works, including
scientific publications. Such protection
is of course provided in the United
States by its Copyright Act. The PMC
deposition requirement does not
undermine copyright protection of the
grantee’s work. Copyrights on works
displayed in PMC are fully enforceable
by the copyright owners. Article 2(1) of
the Berne Convention is consistent with
the widespread practice of reservation
of rights in works by the funders of
those works, which is essentially what
Congress did when it required, as a
condition of a grant award, the
reservation of the right to place a
grantee’s manuscript in PMC. The
concern about the Public Access Policy
and potential conflict with Article 13 of
the WTO TRIPS is unwarranted because
the requirement does not interfere with
the author’s commercial use of the
work. Article 13 directs member
countries to confine limitations on
exclusive rights to special cases that do
10. Evaluation and Impact
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A. Costs to the NIH
Some commenters asked about the
operation and implementation costs of
the policy. By building on an existing
information technology infrastructure
housed at the NLM, the NIH Public
Access Policy is an exceptionally costeffective means to accomplish its goals
of archiving, advancing science, and
enhancing accessibility. At full
compliance, Public Access would cost
the NLM $4.5 million per year (i.e.,
submission of 80,000 articles per year).
Costs may decrease as a greater portion
of journals submit papers directly to
PMC. The NIH spent an additional
$250,000 in fiscal year 2008 in policyrelated staffing costs and contracts, the
Request for Information issuance, and
the March 20 Open Meeting. These costs
will reduce once implementation is
complete. The NIH does not have
estimates on the cost of compliance and
monitoring per grant for NIH staff.
Compliance monitoring may add a few
minutes to managing active projects for
a subset of NIH extramural staff and, as
such, cannot be assigned to a specific
Public Access cost center.
B. Potential Impact on Publishers
Many commenters touched on
potential financial impacts of this Policy
on publishers. Some claimed that the
Policy would be harmful. A subset of
these commenters further argued that if
journals are adversely affected by the
Policy, it would harm peer review as a
whole. No data demonstrating harm to
journals or peer review was submitted.
Some commenters claimed the Policy
would not be harmful to publishers. A
few publishers described their
experience making papers publicly
available at 12 months or less, both on
and off PubMed Central, without
adverse financial impact.
The NIH recognizes the enormous
value and critical role that peer-
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reviewed journals play in the scientific
quality control process. Only peerreviewed papers accepted for
publication will be posted in PMC. This
Policy is designed to preserve the
critical role of journals and publishers
in peer review, editing, and scientific
quality control processes.
As described in FAQ F10, released
September 2008, the NIH is not aware
that there will be a substantial impact of
the policy on Publishers. An increasing
number of journals already provide the
public with free access to the published
article immediately or within one year
of the publication.
The NIH Public Access Policy does
not affect authors’ freedom to choose the
vehicle or venue for publishing their
results. The NIH expects that its
awardees will continue to publish the
results of their research consistent with
their professional autonomy and
judgment in order to advance science as
efficiently and comprehensively as
possible.
The NIH has posted thousands of
papers to PubMed Central under the
NIH Public Access Policy without
evidence of harm to scientific
publishing or to journals. Only a portion
of articles published in scientific
journals result from research funded by
the NIH. Of these articles, only the final
peer-reviewed manuscript is required to
be posted, and it need not be made
publicly available for up to 12 months
post publication. Further, the NIH
continues its practice of allowing
publication costs, including author fees,
to be reimbursed from NIH awards (see
https://publicaccess.nih.gov/
FAQ.htm#e3 for more information).
C. Impact on Science
Many commenters supported the idea
that the policy will support the advance
of science. A few asked for
measurement of these impacts. The NIH
will consider exploring this issue as
compliance rates rise and more NIH
funded papers become available on
PubMed Central. The NIH also
encourages the scientific community to
explore this issue independently.
Changes to Date
In response to the feedback received,
the NIH communications and
procedures regarding the Public Access
Policy have evolved. These changes are
summarized chronologically below.
May 2008
On May 2, 2008, NIH made the
changes listed below to the NIH Public
Access Policy Frequently Asked
Questions (FAQs). These changes
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provide clarifications and do not signify
any changes in policy.
• Questions C7, C9, and C10 are new
and reflect improvements to PubMed.
These clarify and simplify how
awardees can comply with the fifth
specification of the NIH Public Access
Policy, which states: ‘‘Beginning May
25, 2008, anyone submitting an
application, proposal, or progress report
to the NIH must include the PMC or
NIH Manuscript Submission reference
number when citing applicable articles
that arise from their NIH-funded
research. This policy includes
applications submitted to the NIH for
the May 25, 2008, due date and
subsequent due dates.’’
• Questions A4, B10–B12, C8, C11,
D5, E4, E5, F5, and F6 were developed
based on questions received by NIH.
• NIH has responded to a number of
questions about issues already
addressed by the January 11, 2008,
version of the FAQs and has made a
number of small changes to many of
these FAQ questions to improve their
clarity. The biggest changes are in the
wording of FAQs B1–B5.
• The January 11, 2008, FAQ uses the
term ‘‘article’’ as a generic word for a
peer-reviewed scientific publication and
all its versions. At the March 20, 2008,
Open Meeting, some stakeholders
commented that ‘‘article’’ could be
confused with the term ‘‘final published
article.’’ Therefore, this FAQ uses the
term ‘‘paper’’ instead of ‘‘article.’’ The
Web site will be updated to reflect this
change as well.
June 2008
The NIH updated the NIH Manuscript
Submission System (NIHMS) in two
ways:
• Authors, and not Program
Directors/Principal Investigators (PDs/
PIs), now approve manuscripts for
posting. This change reduces the effort
for PDs/PIs who are not authors of
papers that arise from their award. It
also allows these PDs/PIs to more
effectively delegate submission duties to
the author who is most familiar with the
paper. PDs/PIs are now notified by email when a manuscript is linked to one
of their awards via the NIHMS.
• The NIH modified the NIHMS to
allow publishers to fix the delay period
when they submit a manuscript on
behalf of their authors. Authors now
must contact the NIH and their
publisher if they wish to change the
delay. The NIH expects this direct
communication to result in fewer
disagreements about delay periods. In
response to concerns from NIH
employee authors, the NIH developed
procedures its employees can use to
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ensure any manuscripts they write will
be submitted in compliance with the
Public Access Policy. These procedures
are accessible at https://
publicaccess.nih.gov/
nih_employee_procedures.htm.
July 2008
The NIH made several updates to the
NIH Public Access Web page to clarify
the submission process. The Web site
explains that there are four methods to
ensure that a manuscript is submitted to
PubMed Central in compliance with the
NIH Public Access Policy. These
methods vary based on the version of
the paper submitted, and the actions
undertaken by the author and publisher.
Method A: Publish in a journal that
deposits all NIH-funded final published
articles in PubMed Central (PMC)
without author involvement.
Method B: Make arrangements to have
a publisher deposit a specific final
published article in PubMed Central.
Method C: Deposit the final peerreviewed manuscript in PMC yourself
via the NIH Manuscript Submission
System (NIHMS).
Method D: Complete the submission
process for a final peer-reviewed
manuscript that the publisher has
deposited in the NIH Manuscript
Submission System (NIHMS).
August 2008
In response to questions and advice
about identifying PubMed Central
Identifiers (PMCIDs), the National
Library of Medicine created a new
utility (https://www.ncbi.nlm.nih.gov/
sites/pmctopmid) that uses PubMed IDs
(PMIDs) to look up PMCIDs, and vice
versa. Users can enter PMIDs manually
or from their PubMed clipboard. The
utility will provide a table of PMIDs
with corresponding PMCIDs. For
example, an author could look up all
his/her publications in PubMed, save
them to the clipboard, and use the
utility to see which ones have PMCIDs.
September 2008
The Request for Information analysis
indicated that a number of FAQs
developed in support of the previous
voluntary policy remained relevant
under the new Policy requirement.
Accordingly these were slightly
modified and reposted to the FAQs.
They are:
A5. What are the benefits of posting
peer-reviewed papers to PubMed
Central?
F7. Why should there be a public
resource of published peer-reviewed
research findings of NIH-funded
research?
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7613
F8. Rather than archive manuscripts
in NIH’s PubMed Central, why not
provide links to other Web sites?
F9. Aren’t scientific abstracts, which
are currently freely available, sufficient?
Why does the public need full-text
articles?
F10. Will NIH’s Public Access Policy
harm scientific publishing?
F11. Will the NIH Public Access
Policy harm the quality of peer review?
NIH also issued a Guide Notice NOT–
OD–08–119 (https://grants.nih.gov/
grants/guide/notice-files/NOT-OD-08119.html) informing PDs/PIs and
Institutional Business Officials that they
may receive e-mails from NIH staff if
their applications, proposals, or reports
appear to be noncompliant with the NIH
Public Access Policy. The Guide Notice
also provides reminders about the
instructions for citing literature in key
NIH forms (e.g., the PHS398, SF424,
PHS2590) and through eSNAP.
Current Status
The NIH Public Access Policy
requirement took effect April 7, 2008,
during the Request for Information, and
after the Open Meeting. The NIH made
a number of improvements based on the
feedback it was receiving; the results of
these efforts appear promising. The
months following April 7, 2008, have
been marked by increased participation
from both publishers and authors,
which has led to increased collection
rates for eligible papers.
The NIH estimates that approximately
80,000 papers arise from NIH funds
each year, and this total serves as the
target for the Public Access Policy. One
can gauge the progress of the
implementation of the mandatory Policy
by comparing the percentage of NIHfunded papers collected in the period
April 2008 to August 2008 with the rate
that was achieved under the voluntary
Policy (May 2005 to December 2007).
As described at https://
publicaccess.nih.gov/
submit_process.htm, the NIH provides
four methods for submitting papers
under the Policy. With two of these
(methods A and B) publishers
voluntarily submit final published
articles directly to PubMed Central.
With the other two, (methods C and D)
authors and publishers can submit final
peer-reviewed manuscripts to PMC via
the NIH Manuscript Submission System
(NIHMS). As Figure 1 indicates, the
estimated percentage of final published
articles submitted directly to PubMed
Central (methods A and B) has more
than doubled under the new
requirement as compared to the earlier
voluntary policy. Rates rose from 12
percent to 26 percent.
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The percentage of manuscripts
collected via the NIH Manuscript
Submission System (NIHMS, using
methods C and D) more than
quadrupled, from 7 percent under the
voluntary policy to an estimated 30
percent under the requirement.
Overall, the Public Access success
rate rose from 19 percent of all NIHfunded papers to 56 percent of all NIHfunded papers after the requirement
took effect. These first five months show
the promise of a Public Access Policy
requirement, though the NIH and its
awardees remain over 40 percent short
of their statutory obligation to make
NIH-funded papers available on
PubMed Central. Also, while the NIH
expects to post all 56 percent of these
NIH papers, most of them will not be
publicly available until 2009.
Future Activities
The NIH expects to continually
monitor and refine the communications
and procedures surrounding the NIH
Public Access Policy. These changes
will be governed by advice and feedback
from stakeholders, questions to the help
desk, and paper collections rates.
The NIH is exploring ways to enhance
the utilities on PubMed and integrate
them with bibliographic information on
the eRA Commons Profile. For example,
NLM just updated its search
management tool (https://
www.ncbi.nlm.nih.gov/sites/myncbi/).
This service could eventually provide a
way for PDs/PIs and other authors to
track their papers that arise from NIH
funds, associate them with NIH awards,
and automatically obtain PMCIDs as
they become available.
The NIH also is exploring ways to
facilitate the reporting of papers arising
from NIH awards by NIH project
number. These services will help
investigators and their institutions
monitor compliance policy.
The NIH looks forward to continued
interaction and advice from the many
public access stakeholders. Comments
and questions may be directed to
PublicAccess@NIH.gov.
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Note: a full version of this report is
available at https://publicaccess.nih.gov/
analysis_of_comments_nih_public_access_
policy.pdf.
Dated: February 10, 2009.
Raynard S. Kington,
Acting Director, National Institutes of Health.
[FR Doc. E9–3442 Filed 2–17–09; 8:45 am]
BILLING CODE 4140–01–P
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2), notice
is hereby given of the following
meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, ELSI
Microbiome.
Date: February 27, 2009.
Time: 1:30 p.m. to 6:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Richard A. Currie, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 1108,
MSC 7890, Bethesda, MD 20892, (301) 435–
1219, currieri@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
Name of Committee: Center for Scientific
Review Special Emphasis Panel,
Cardiovascular Devices.
Date: March 2, 2009.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Bahia Resort Hotel, 998 W. Mission
Bay Drive, San Diego, CA 92109.
Contact Person: Roberto J. Matus, MD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5108,
MSC 7854, Bethesda, MD 20892, 301–435–
2204, matusr@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Disease
Models, Astrocytes, and Neurodegeneration.
Date: March 3–5, 2009.
Time: 3 p.m. to 3 p.m.
Agenda: To review and evaluate grant
applications.
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Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Joanne T. Fujii, PhD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4184,
MSC 7850, Bethesda, MD 20892, (301) 435–
1178, fujiij@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Member
Applications for Nursing Sciences.
Date: March 6, 2009.
Time: 1 p.m. to 3 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Ellen K. Schwartz, EDD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3168,
MSC 7770, Bethesda, MD 20892, 301–435–
0681, schwarte@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
Name of Committee: AIDS and Related
Research Integrated Review Group, AIDSassociated Opportunistic Infections and
Cancer, Study Section.
Date: March 9, 2009.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: The Fairmont Washington, DC, 2401
M Street, NW., Washington, DC 20037.
Contact Person: Eduardo A. Montalvo,
PhD, Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5108,
MSC 7852, Bethesda, MD 20892, (301) 435–
1168, montalve@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Technology
Centers for Networks and Pathways.
Date: March 9–10, 2009.
Time: 8 a.m. to 1 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hotel Kabuki, 1625 Post Street, San
Francisco, CA 94115.
Contact Person: Marc Rigas, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5158,
MSC 7849, Bethesda, MD 20892, 301–402–
1074, rigasm@mail.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Member
Conflict Special Emphasis Panel.
Date: March 9–10, 2009.
Time: 8 a.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Rass M. Shayiq, Ph.D.,
Scientific Review Officer, Center for
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[Federal Register Volume 74, Number 31 (Wednesday, February 18, 2009)]
[Notices]
[Pages 7603-7614]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-3442]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Analysis of Comments and Implementation of the NIH Public Access
Policy
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
Background
The National Institutes of Health (NIH) Public Access Policy
requires investigators funded by the NIH to submit, or have submitted
for them, an electronic version of their final, peer-reviewed
manuscripts upon acceptance for publication to the National Library of
Medicine's digital archive, PubMed Central, to be posted publicly
within 12 months after the official date of publication. Congress
required the NIH to implement this funding limitation in Division G,
Title II, Section 218 of the Consolidated Appropriations Act of 2008
(``Section 218''). The Policy is intended to advance science, provide
public access to the published results of NIH-funded research, and
improve human health.
The current Public Access Policy is the culmination of years of
effort and community interaction. Prior to passage of Section 218, the
NIH undertook extraordinary public outreach concerning the issue of
public access to the published results of NIH-funded research. These
outreach efforts included a review of over six thousand public comments
and the establishment of an independent advisory group to review NIH's
implementation of a voluntary Public Access Policy. Additionally, as
part of the process to implement Section 218 in a transparent and
participatory manner, the NIH formally sought public input through an
open meeting and a Request for Information (RFI) seeking public
comment. This open meeting occurred on March 20, 2008, and was designed
to ensure that a discussion of stakeholder issues could occur. The
feedback from the open meeting helped define questions for an RFI,
which was published on the NIH Web site on March 28, 2008 and in the
Federal Register on March 31, 2008 (73 FR 16881-16895). The RFI was
designed to seek input on the NIH Public Access Policy, as it was
revised to incorporate Section 218, and the responses to frequently
asked questions (FAQs) concerning it. The RFI was open for sixty days
following publication in the Federal Register, from March 28 to May 31,
2008.
[[Page 7604]]
Overview of Feedback
In response to the open meeting and RFI, the NIH received 613
unduplicated comments from a broad cross-section of the public,
including NIH-funded investigators, members of the general public,
patient advocates, professional organizations, and publishers. This
report summarizes these comments.
Most comments offered broad support for the policy as written. Many
comments requested a reduction in the delay period before papers can be
made publicly available on PubMed Central. In some cases, commenters
expressed concern about the Policy, others asked for clarification, and
still others suggested alternatives to NIH's implementation. These
questions and concerns fall into several broad categories:
The potential administrative burden on Program Directors/
Principal Investigators and awardee institutions.
The details of implementing the Policy, including
applicability, cost reimbursement, compliance monitoring and
enforcement, and publisher support of the Policy.
Associated issues, such as submission procedures, tracking
submitted papers, version of the paper submitted, and managing and
protecting copyrights.
The accordance of the Policy Implementation with copyright
law and the Administrative Procedures Act.
Questions about Policy impact, such as financial impacts
on publishers and NIH.
The NIH also received comments describing implementation efforts by
numerous awardee institutions and publishers. In some cases, libraries
took the lead on educating their faculty and supporting them in
interpreting publishing agreements and submitting manuscripts to NIH.
In other cases, offices of sponsored research provided guidance on the
NIH Public Access Policy disseminated to their faculty community via
the Web, memos, seminars, and video casts. Still other institutions
described collaborations between libraries, offices of sponsored
research, university counsels, and technology transfer offices. Several
universities and private groups described the development of new
policies on scholarly communications and new publishing forms and
addenda that their faculty could use to ensure compliance with the
Policy.
NIH Response
The NIH carefully considered the views expressed by publishers,
patient advocates, scientists, university administrators, and others in
the comments submitted. Throughout the course of its analysis, the NIH
undertook various efforts to respond to concerns as it identified them.
The agency aimed these actions to clarify the Public Access Policy and
to facilitate compliance with Section 218. In May, July, and September
of 2008, NIH updated the Public Access Web site to clarify the
applicability, goals and anticipated impact of the policy, the
available methods to submit papers, and planned methods to document
compliance. In June 2008, NIH updated the NIH Manuscript Submission
System (NIHMS), the online mechanism for submission of manuscripts to
PubMed Central (PMC), to allow Program Directors/Principal
Investigators (PDs/PIs) to delegate all aspects of submission tasks to
authors, and to allow publishers who submit manuscripts to the NIHMS on
behalf of authors to exert greater control over manuscript delay
periods. In August, the National Library of Medicine issued a new Web
tool to help the scientific community obtain PubMed Central Identifiers
in bulk. In September 2008, NIH issued a Guide Notice (NOT-OD-08-119 at
https://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-119.html)
reminding awardees about the compliance process and providing details
concerning NIH's monitoring plan for fiscal year 2008.
These efforts appear to be working. The NIH estimates approximately
80,000 papers arise from NIH funds each year, and this total serves as
the target for the Public Access Policy. During the voluntary policy,
from May 2005 to December 2007, the NIH was able to collect a total of
19 percent of targeted papers, from all sources. Under the first five
months of the Section 218 requirement (April to August 2008), this rate
jumped to an estimated 56 percent of papers per month. While NIH
expects to post all of the estimated 56 percent of these NIH papers,
most of them will not be publicly available until 2009.
These first few months show the promise of a Public Access Policy
requirement, its implementation, and the active support from the
academic and publishing communities. However, work still remains as
over 40 percent of applicable papers per month remain unsubmitted.
Implementation and process refinement will be continuing in the
coming months. The NIH has established voluntary partnerships with many
publishers to facilitate deposit of manuscripts and final published
papers and expects these partnerships to continue to expand and the
percentage of submitted papers to grow. The NIH will also continue to
engage the community as we proceed to implement the Policy in the most
efficient and effective manner possible.
Policy Overview
The NIH Public Access Policy, announced in January 2008, ensures
that the public has access to the published results of NIH-funded
research. See https://grants.nih.gov/grants/guide/notice-files/NOT-OD-
08-033.html. It requires scientists to submit final peer-reviewed
journal manuscripts that arise from NIH funds to the digital archive
PubMed Central upon acceptance for publication. To help advance science
and improve human health, the Policy requires that these papers be
accessible to the public on PubMed Central no later than 12 months
after publication.
This Policy implements the Consolidated Appropriations Act of 2008,
which directed the NIH to require investigators funded by the NIH to
submit, or have submitted for them, an electronic version of their
final, peer-reviewed manuscripts upon acceptance for publication to the
National Library of Medicine's digital archive, PubMed Central (PMC),
to be posted publicly within 12 months after the official date of
publication. The Policy builds upon the experience with NIH's voluntary
Public Access Policy, which was published in 2005 and has three aims:
1. ARCHIVE. A central collection of NIH-funded research
publications preserves vital published research findings for years to
come.
2. ADVANCE. The archive is an information resource for scientists
to research publications and for NIH to manage better its entire
research investment.
3. ACCESS. The archive makes available to the public research
publications resulting from NIH-funded research.
Policy History
The original, voluntary Public Access Policy, implemented May 2005
(NOT-OD-05-022, available at https://grants.nih.gov/grants/guide/notice-
files/NOT-OD-05-022.html), encouraged but did not require investigators
receiving NIH funding to deposit their peer-reviewed manuscripts into
PubMed Central. It was shaped, in large part, through discussion with
the extramural community.
The NIH began public discussions on this topic with three town hall
style meetings in 2004. From this feedback, the NIH developed a
proposal for a voluntary public access policy that would make final
peer-reviewed
[[Page 7605]]
manuscripts publicly available on PubMed Central within 6 months of
publication. The NIH issued the proposed NIH Public Access Policy for
comment in September 2004 (see https://grants.nih.gov/grants/guide/
notice-files/NOT-OD-04-064.html or https://a257.g.akamaitech.net/7/257/
2422/06jun20041800/edocket.access.gpo.gov/2004/04-21097.htm). In
response to its request for input on the proposed policy, NIH received
over 6,200 comments from interested parties, including grantees,
publishers and trade organizations. After carefully considering all the
comments received, the NIH published a final policy, NOT-OD-05-022, on
February 3, 2005 (also published at 70 FR 6891). Though 66 percent of
comments favored a six-month delay period, the NIH implemented a
voluntary Public Access policy with a 12-month delay period out of
deference to concerns from some members of the publishing community.
Implementation of this voluntary policy was marked by continued
engagement with multiple stakeholders in order to facilitate
participation. The NIH staff met dozens of times and exchanged hundreds
of letters with patient advocacy groups, awardee institutions and their
representatives, publishers, and scientific societies regarding the
Policy. (For a breakdown of meetings and correspondence, see slide 12
of NIH Director Elias Zerhouni's presentation at the March 20, 2008,
open meeting at https://publicaccess.nih.gov/comments/Overview_
Context.pdf.) In collaboration with publishers, investigators,
grantees, and others, the NIH established systems to make it easy for
scientists to deposit their manuscripts directly and for interested
publishers to deposit manuscripts on scientists' behalf. For example,
the NIH Manuscript Submission System (NIHMS), a Web service built to
support the Policy, allows publishers to submit manuscripts on behalf
of authors in bulk. The NIH also developed new forms of PubMed Central
Journal agreements in collaboration with publishers, which enable
publishers to submit final, published articles to PubMed Central from
NIH-funded authors, only and/or from authors who pay open access fees
to the journals.
Thus, for almost three years, the NIH asked the scientists it
supports to deposit their NIH-funded scientific manuscripts in an NIH
online system that would make them accessible to the public, freely and
in perpetuity. But the compliance rate under the voluntary system
demonstrated that it would not achieve the goals of the Public Access
Policy. In December 2007, the Consolidated Appropriations Act of 2008
was signed into law, directing the NIH to require submission of
manuscripts.
Implementing the Consolidated Appropriations Act of 2008
The Consolidated Appropriations Act of 2008 (Pub. L. 110-161), at
Division G, Title II, Section 218, directs the NIH as follows: The
Director of the National Institutes of Health shall require that all
investigators funded by the NIH submit or have submitted for them to
the National Library of Medicine's PubMed Central an electronic version
of their final, peer-reviewed manuscripts upon acceptance for
publication, to be made publicly available no later than 12 months
after the official date of publication: Provided, that the NIH shall
implement the public access policy in a manner consistent with
copyright law.
On January 11, 2008, NIH issued the Public Access Policy
implementing this clear and unambiguous new statute. As described in
the NIH Guide for Grants and Contracts (NOT-OD-08-033, available at
https://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-033.html),
the Policy restates the statute and offers the following specifics:
1. The NIH Public Access Policy applies to all peer-reviewed
articles that arise, in whole or in part, from direct costs \1\ funded
by NIH, or from NIH staff, that are accepted for publication on or
after April 7, 2008.
---------------------------------------------------------------------------
\1\ ``Directly'' funded means costs that can be specifically
identified with a particular project or activity. See NIH Grants
Policy Statement, Rev. 12/2003.
---------------------------------------------------------------------------
2. Institutions and investigators are responsible for ensuring that
any publishing or copyright agreements concerning submitted articles
fully comply with this Policy.
3. PubMed Central (PMC) is the NIH digital archive of full-text,
peer-reviewed journal articles. Its content is publicly accessible and
integrated with other databases (see: https://www.pubmedcentral.nih.gov/
).
4. The final, peer-reviewed manuscript includes all graphics and
supplemental materials that are associated with the article.
5. Beginning May 25, 2008, anyone submitting an application,
proposal, or progress report to the NIH must include the PMC or NIH
Manuscript Submission reference number when citing applicable articles
that arise from their NIH-funded research. This policy includes
applications submitted to the NIH for the May 25, 2008 due date and
subsequent due dates.
Compliance
Compliance with this Policy is a statutory requirement and a term
and condition of the grant award and cooperative agreement, in
accordance with the NIH Grants Policy Statement. For contracts, the NIH
includes this requirement in all R&D solicitations and awards under
Section H, Special Contract Requirements, in accordance with the
Uniform Contract Format.
In addition to announcing the Policy, the NIH established a Web
site and posted responses to frequently asked questions (FAQs) that
provide authors, their institutions, and their publishers with guidance
on the implementation of the policy.
As part of the process to implement Section 218 in a transparent
and participatory manner, the NIH formally sought public input through
an open meeting and a Request for Information seeking public comment.
The open meeting occurred on March 20, 2008 (NOT-OD-08-057), and was
designed to ensure that discussion of stakeholder issues could occur.
The feedback from the open meeting helped define questions for a
Request for Information (RFI), conducted from March 28 to May 31 (NOT-
OD-08-060). This report summarizes comments received at the meeting and
in response to the RFI.
Open Meeting
The purpose of the Thursday, March 20, 2008, meeting was to seek
comment from the public on implementation of the NIH Public Access
Policy. The meeting was open to all, including NIH-funded researchers,
representatives of universities and other NIH grantee organizations,
publishers (including commercial organizations, professional societies,
and journal editors), patients and public health advocates, and members
of the general public. The NIH desired broad participation and
commentary.
In particular, the NIH was interested in input concerning the
Public Access Policy and the effectiveness of the policy's
implementation. Individuals, groups, and organizations were also
invited to submit written pre-meeting comments on the NIH Policy.
The NIH made every effort to make the meeting and pre-meeting
comments open and transparent. Comments were made public as they were
received. The meeting was video cast, and everyone who wished to speak
was able to. All meeting materials, including the Guide Notice, Federal
Register Notice, video cast, transcript, and comments are available at
https://publicaccess.nih.gov/open_meeting_march_2008.htm.
[[Page 7606]]
Comments posted on this site are recorded as submitted and, in some
cases, include duplicates.
Request for Information (RFI)
The feedback from the open meeting helped define questions for a
Request for Information (RFI), which was published on the NIH Web site
on March 28, 2008, and in the Federal Register on March 31, 2008 (73 FR
1681-1695) (see NOT-OD-08-060). The NIH sought information from the
public, including all stakeholders, about the new NIH Public Access
Policy and the frequently asked questions developed to assist
investigators to implement it. Among other issues, the NIH particularly
sought information about the following questions:
Do you have recommendations for alternative implementation
approaches to those already reflected in the NIH Public Access Policy?
In light of the change in law that makes NIH's public
access policy mandatory, do you have recommendations for monitoring and
ensuring compliance with the NIH Public Access Policy?
In addition to the information already posted on the NIH
Web site, what additional information, training or communications
related to the NIH Public Access Policy would be helpful to you?
Individuals, groups, and organizations interested in responding
were invited to do so via a Web site that would record their responses
for each question and make those responses publicly available. All
comments received via the Web and e-mail related to the Public Access
Policy RFI is now available at https://publicaccess.nih.gov/
comments.htm.
Methodology for Analysis
Consolidating and Categorizing Comments
Comments were posted as they were collected, and commenters had the
opportunity to respond to other comments. This was a deliberate effort
on the part of NIH to encourage dialogue among stakeholders and to
provide a more synthesized set of ideas for analysis. Individuals and
organizations were allowed to submit multiple comments, and all
comments were treated equally, regardless of the source. Although the
NIH requested input on several open-ended questions at the meeting and
in the RFI, commenters did not restrict themselves to input on these
questions and offered a variety of opinions on other topics, either in
addition to responding to the questions or in lieu of responding to
them.
Combined, the open meeting and RFI yielded 613 unduplicated
comments. The comments include materials entered through the online
comment service, transcriptions of in-person statements offered at the
March 20 Open Meeting, and e-mails received at the Public Access
comments mail box.
Duplicates were identified by finding multiple comments from the
same individual that contained identical content. Comments that were
entirely off-topic (e.g., SPAM, selling products) were considered
nonresponsive and thus not counted. If an individual submitted multiple
responses and each submission contained new content, they were not
marked as duplicates and were separately counted and analyzed. In
addition, if the same comment or information (e.g., a form letter) was
received from two or more individuals those comments were counted
separately and not marked as duplicates.
All unduplicated comments underwent an initial review to identify
the topic(s) addressed and to gain a sense of the relative number of
commenters who addressed each topic. This initial analysis helped to
identify major themes for inclusion in this report.
The 613 unduplicated comments covered by this report, combining
comments from both the open meeting and the RFI, and including PDF
comments converted to text using optical character recognition, became
available in a single file at https://publicaccess.nih.gov/comments.htm
in October 2008. We invite our stakeholders to use these resources to
conduct independent analyses of these data.
The public comments were largely supportive of the Policy. Comments
clustered around several broad themes. We describe them below, followed
by NIH's analysis and response where appropriate.
1. Need for the Policy
The most common theme among comments, expressed in a large majority
of all comments, was support for the Policy as written. When reasons
for support were offered, the most common were as follows: (1) The
perceived benefit to patients and their families, (2) the belief that
the American public has a right to access papers arising from NIH
funds, and (3) the expected potential of the policy to advance
scientific discovery. A small minority of comments expressed general
disagreement with the Policy and/or felt that increasing access to
papers arising from NIH funds was unnecessary.
2. The Length of the Delay Period
The second largest number of comments, second only to general
support for the Policy, were comments advocating reducing the period of
time before papers are made publicly available on PubMed Central. A
large number of commenters argued for a shorter maximum delay period--
many suggested 6 months, many no delay period at all, and a few
suggested 3 months. Advocates for reducing the period of time explained
that doing so would provide greater benefits to the public and to
science. Some further claimed, and provided examples of how, shorter
delay periods would not harm publisher interests. A few commenters
suggested that the maximum delay period should be greater than 12
months. These commenters claimed that a longer delay period was needed
to protect journals in certain disciplines.
The NIH appreciates the concerns of all commenters concerning the
maximum delay period between journal publications and posting on PubMed
Central. The Consolidated Appropriations Act of 2008 specifies the
maximum delay period at 12 months. Copyright holders may always post
materials with a shorter delay period, at their discretion.
3. Actions Taken by Institutions to Support Implementation
Many commenters shared their efforts to implement and promote the
Policy. Several publishers described their efforts to support
implementation, either by facilitating submission of papers on behalf
of their authors, or by offering new guidance and publishing agreements
so that their authors may understand how to comply with the Policy.
A number of awardee institutions offered their implementation
strategies as well. In some cases, libraries were taking the lead in
educating their faculty and supporting them in interpreting publishing
agreements and submitting manuscripts to the NIH. In other cases,
offices of sponsored research described guidance on the NIH Public
Access Policy disseminated to their faculty community via the Web,
memos, seminars, and video casts. Still other institutions described
collaborations between libraries, offices of sponsored research,
university counsel, and technology transfer offices. Several
universities and private groups also described institutional policies
on scholarly communication and new publishing forms and addenda that
their
[[Page 7607]]
faculty could use to ensure compliance with the Policy.
The NIH is interested in the role institutions may play in
supporting the Policy and appreciates the efforts of these commenters
to both support the policy and share their strategies. In January 2008,
the NIH published an article outlining key questions institutions may
wish to consider as they implement the Policy (https://grants.nih.gov/
grants/partners/0108Nexus.htm#investigator). Based on the comments
submitted, it appears that the community has developed multiple
approaches to issues described in this article, but it is too early in
the implementation of the Policy to determine if some approaches are
more successful than others.
NIH employees publish several thousand peer-reviewed papers each
year, and the NIH has to support the Policy as an investigator
institution as well. Our approach to ensure compliance among our own
faculty involves support from the NIH Library, a unit of the NIH Office
of Research Services; NIH technology transfer representatives; and the
NIH Office of Intramural Research. The NIH offers employees guidance on
our Web site, a publishing agreement addendum, centralized negotiation
of publishing agreements, help desk support for manuscript submission
and policy questions, and staff training upon request. See https://
publicaccess.nih.gov/nih_employee_procedures.htm for more
information.
4. Administrative Burden for Institutions and Principal Investigators
Some comments expressed concern that the Policy would create undue
burdens on authors, investigators, and institutions. The comments are
described below.
A. Negotiating Publisher Agreements
Some comments suggested the Policy required authors and individual
investigators to negotiate with publishers directly. They felt
individual authors lacked the skills or bargaining power to develop an
agreement with a publisher that met their needs under the Policy.
Investigators are central to implementing the Policy and usually
are the initial copyright holder of the manuscripts that fall under the
Policy. They may need to negotiate the terms of publishing agreements
with publishers directly. However, the NIH expects that institutions
will support their investigators in complying with terms and conditions
of award. The NIH Public Access Policy states ``Institutions and
investigators are responsible for ensuring that any publishing or
copyright agreements concerning submitted articles fully comply with
this Policy.'' The NIH underscores the importance of institutional
support throughout the Frequently Asked Questions (FAQ). For example,
FAQ C4 addresses publishing agreements or publishers that may not
support compliance with the Policy. FAQ C11, released in May 2008 in
response to this feedback, addresses another aspect of this concern. In
both cases, the NIH encourages authors and investigators to work with
their institution's office of sponsored research.
With regard to particular agreement terms, individual copyright
arrangements can take many forms, and authors and their institutions
should continue to manage such arrangements as they have in the past.
Institutions and investigators may wish to develop particular
copyright agreement terms in consultation with their own legal counsel
or other applicable official at their institution, as appropriate. As
an example, the kind of language that an author or institution might
add to a copyright agreement includes the following (as described in
FAQ C3):
``Journal acknowledges that Author retains the right to provide a
copy of the final peer-reviewed manuscript to the NIH upon acceptance
for Journal publication, for public archiving in PubMed Central as soon
as possible but no later than 12 months after publication by Journal.''
There are many other potential models, some of which were described
in other comments and are available for viewing therein.
B. Ability for Investigators to Publish in the Journal of Their Choice
A few comments expressed concern that some journals would refuse to
allow manuscripts to be posted to PMC in accordance with the Policy,
and authors would not be able to publish in those journals. They
claimed this could occur despite an author's best efforts to negotiate
with a publisher.
The NIH agrees that author choice of publication is a very
important issue, but if this situation were to occur, an author might
have to find an alternate journal. Therefore, the NIH encourages
authors to clearly communicate with and address these issues before
they may transfer their copyright and potentially lose their ability to
comply with the Policy. The Public Access Home page states: ``Before
you sign a publication agreement or similar copyright transfer
agreement, make sure that the agreement allows the paper to be
submitted to NIH in accordance with the Public Access Policy.''
The NIH has also engaged the publishing community in order to
minimize copyright concerns when possible. The NIH has established
voluntary partnerships with many publishers who agree to facilitate
deposit of manuscripts and final published papers. The number of papers
submitted via these agreements has grown since the Public Access Policy
took effect. The NIH issued guidance to authors to clarify these
various arrangements in July 2008. The guidance can be found at https://
publicaccess.nih.gov/submit_process.htm. Whether because of NIH's
direct efforts, clear communication from authors and institutions or
because of publisher support for the Policy, NIH did not receive
comments indicating that publishers or publishing agreements have
actually prevented authors from complying with the Policy. To the best
of our knowledge, this concern currently remains a hypothetical risk
and not a manifest problem.
C. Cost Reimbursement
Some commenters raised the issue of investigators or awardees
needing to pay potential publishing costs and fees associated with the
Policy (e.g., fees for posting to PubMed Central, fees to reduce delay
periods). Some commenters suggested that the NIH should cover these
costs, others requested clarification concerning costs, and still
others thought the NIH would offer no financial support to either
institutions or publishers. As such, the commenters felt that the
Policy was an unfunded mandate that might harm author or publisher
interests, with junior authors (new investigators and trainees) being
especially vulnerable. However, several commenters thought any
unrecovered costs associated with the Policy were worth the benefits,
and one commenter even requested that the NIH stipulate that costs not
be covered.
As with other costs, the NIH will reimburse publication costs,
including author fees, for grants and contracts on three conditions:
(1) Such costs incurred are actual, allowable, and reasonable to
advance the objectives of the award; (2) costs are charged consistently
regardless of the source of support; (3) all other applicable rules on
allowability of costs are met. Generally, page charges for publication
in professional journals are allowable if the published paper reports
work supported by the grant and the charges are levied impartially on
all papers published by the journal,
[[Page 7608]]
whether or not they are submitted by Government-sponsored authors.
D. Compliance Burden
Some commenters expressed concern about the time Program Directors/
Principal Investigators (PDs/PIs) and authors will need to spend to
submit papers. A few commenters said that a simple submission system
was critical to the success of the policy. Among those commenting on
the potential burden of the submission process, a portion said the
existing NIH Manuscript Submission System (NIHMS) was easy to use, a
portion said it was complex and burdensome, and a portion were unaware
of how it worked. Some commenters also expressed concern or offered
suggestions related to the notification and management of PubMed
Central Identifiers (PMCIDs), which are assigned to papers after they
are submitted and can be used to demonstrate compliance with policy on
applications, proposals, and reports.
The NIH agrees with the need to have a simple manuscript submission
process to minimize the time associated with deposit of manuscripts
into PubMed Central. NIH has worked diligently since the adoption of
the voluntary Public Access Policy in 2005 to develop a streamlined and
efficient process. During the voluntary Policy, NIH found it took
authors about 10 minutes to deposit a paper in the NIH Manuscript
Submission System (NIHMS); the time decreased for submitters as they
began to submit more papers and gained experience with the system.
The NIH continues to refine the NIHMS as necessary. For example,
starting in June 2008, NIH eliminated the need for PDs/PIs to review
each deposit. Instead, the NIHMS now allows authors to complete all
aspects of manuscript submission, with the idea that greater
flexibility in delegation will minimize PD/PI burden. The NIH gives
specific guidance on these submission processes on its Web site at
https://publicaccess.nih.gov/submit_process.htm. This guidance also
describes how authors can delegate some submission tasks to someone in
the author's organization (e.g., an assistant or a librarian), or to
their publisher, and how all aspects of submission can be delegated to
a publisher that participates in PubMed Central.
The NIH has developed Policy compliant alternatives to manuscript
deposit that require less author effort. For example, as described at
https://publicaccess.nih.gov/submit_process.htm, some publishers sign
agreements with the NIH to submit final published articles directly to
PubMed Central without author involvement. Since the passage of the
2008 Consolidated Appropriations Act, the number of publishers signing
such agreements has significantly increased.
The NIH has also made changes to the way it reports PubMed Central
reference numbers (PMCID), and how authors and delegates can use the
NIHMS system. For example, as described in FAQ C9, issued May 2008, the
PMCID is posted in PubMed as soon as an article has been successfully
processed by PMC, which usually occurs around the time of publication.
PMCIDs are listed in the lower right corner of the Abstract Plus view
of PubMed (https://www.ncbi.nlm.nih.gov/PubMed/). If the paper is not
yet publicly available on PMC, PubMed will also list the date the paper
will become available. The NIH provides other methods of obtaining
PMCIDs (e.g., https://www.ncbi.nlm.nih.gov/sites/pmctopmid, created in
August 2008), as do several bibliography management software packages.
E. Collaborations With Institutional Repositories
As a way to relieve compliance burdens on their faculty, a few
institutions requested direct feeds from their repositories to PubMed
Central or the NIH Manuscript Submission system.
The NIH believes that these are worthwhile suggestions, but it is
concerned that they raise important technical and logistical challenges
regarding author approval, copyright permissions, quality control, and
formats for electronic transfer. The NIH remains open to closer
collaboration with institutional archives and will consider this issue
as the Policy matures. National Library of Medicine representatives met
with representatives from academic communities to discuss this issue in
November 2008.
5. Expanding the Scope of the Public Access Policy
Some commenters suggested the Policy be expanded in several ways
from investigators and research funded by additional or all Federal
research funds to papers published before April 7, 2008, or to the data
and unpublished results associated with an award. A few comments
suggested a specific alternative approach to expand the scope of the
policy to exempt all works arising from NIH/Government funds from
copyright protection.
The NIH understands and appreciates the strongly held views of many
commenters concerning access to works funded by the NIH and the
Government generally. The NIH Public Access Policy implements the
Consolidated Appropriations Act of 2008, Division G, Title II, Section
218 (Pub. L. 110-161), a Federal statute that was passed by Congress
and signed by the President of the United States. This statute is very
specific--it indicates what is to be submitted and when, and when and
where submissions are made publicly available.
The NIH's new Access Policy took effect a few months after passage
of the law to allow copyright holders to make arrangements to post
directly and in accordance with copyright law. Regarding the suggestion
that works funded through the NIH should be denied copyright
protection, we note that works of Government employees, including NIH
investigators, are not subject to copyright protection in the United
States (17U.S.C. 105). The works of Government awardees, however, are
subject to copyright protection.
6. Issues About the Policy and Its Implementation Requiring
Clarification
A number of issues were raised that resulted in NIH providing
clarifications.
A. Compliance Monitoring and Enforcement
A number of comments suggested that investigators should include
evidence of compliance with the Policy in applications, proposals or
reports submitted to the NIH. A few comments simply asked what is the
process for enforcing compliance.
It is unclear whether the commenters proposing reference within NIH
applications, proposals, or reports were endorsing the Policy as
implemented, as it already specifies that investigators should do so,
or were unaware of the compliance procedure described in the January
11, 2008 Guide notice. As is made clear therein, the NIH expects that
investigators citing their NIH-funded papers subject to the Policy in
NIH applications, proposals, or progress reports will include the
PubMed Central reference number for each applicable paper.
The NIH clarified the compliance reporting process with an update
to the Web site in May 2008 and further clarified the compliance
documentation and monitoring processes in a Guide Notice (OD-NOT-08-119
at https://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-119.html).
FAQ C8, also part of the May 2008 release, clarifies that the Policy
reporting requirement for applicants and PDs/PIs only applies to papers
that are authored by them or arose from their NIH award and fall under
the policy.
[[Page 7609]]
Some commenters also asked about consequences for PDs/PIs and
institutions if manuscripts are not submitted as required by the law
and the Policy. Generally, and as specified in the NIH Guide for Grants
and Contracts, a grantee's failure to comply with the terms and
conditions of award may cause the NIH to take one or more enforcement
actions, depending on the severity and duration of the noncompliance.
The NIH will undertake any such action in accordance with applicable
statutes, regulations, and policies. The NIH generally will afford the
grantee an opportunity to correct the deficiencies before taking
enforcement action unless public health or welfare concerns require
immediate action. However, even if a grantee is taking corrective
action, the NIH may take proactive action to protect the Federal
Government's interests, including placing special conditions on awards
or precluding the grantee from obtaining future awards for a specified
period, or may take action designed to prevent future noncompliance,
such as closer monitoring. See Enforcement Actions in the NIH Grants
Policy Statement (11/03): https://grants.nih.gov/grants/policy/nihgps_
2003/NIHGPS_Part8.htm#_Toc54600145.
B. Preventing Copyright Violations on PMC
The NIH received feedback on the potential copyright implications
of posting papers to PubMed Central (PMC), which cluster into two
themes. Some comments asked how the NIH will prevent inappropriate
posting of materials to PMC without permission of the copyright holder
or posting prior to expiration of the delay period specified by the
submitter. Other comments, described below, expressed concern about the
operation of PMC and the protections it offers copyright holders
against inappropriate use of their works.
The comments about inappropriate posting primarily focused on
individuals posting content without copyright permission. The NIH
manuscript submission system is the only way in which authors may
deposit manuscripts to PMC. That process requires the author to confirm
he or she has the right or permission for the specific version
submitted to be posted to PMC after the specific delay period.
Publishers and authors have occasionally disagreed on the terms of
their publishing agreements. Publishers have submitted final peer-
reviewed manuscripts on behalf of their authors requesting a specific
delay period, and in the course of approving the manuscript for
posting, authors have selected a shorter delay period. In June 2008,
NIH modified the NIH Manuscript Submission System to allow a publisher
to fix the delay period when they submit a manuscript on behalf of
their authors. Authors now have to contact NIH and their publisher if
they wish to change the delay. We expect this more direct communication
will result in fewer disagreements about delay periods.
Commenters also asked how NIH safeguards privately copyrighted
materials on PubMed Central once it is posted. NIH has eight years of
experience in safeguarding copyrighted material on the PMC Web site,
the host archive of the Public Access Policy. There are over 1.5
million full-text articles on the Web site. PMC has algorithms to
detect inappropriate use, such as bulk downloading, and sites
responsible for inappropriate use are warned of the consequences of
violating copyright provisions and blocked from further access.
C. Applicability of the Policy
Some commenters asked questions or expressed confusion about the
papers to which the Policy applies. Applicability was clarified in the
May 2008 FAQ B1. The Policy applies to any manuscript that:
Is peer-reviewed;
And, is accepted for publication in a journal on or after
April 7, 2008.
And, arises from:
Any direct funding \2\ from an NIH grant or cooperative
agreement active in fiscal year 2008, or;
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\2\ ``Directly'' funded means costs that can be specifically
identified with a particular project or activity. See NIH Grants
Policy Statement, Rev. 12/2003.
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Any direct funding from an NIH contract signed on or after
April 7, 2008, or;
Any direct funding from the NIH Intramural Research
Program, or;
An NIH employee.
Consistent with the NIH's long-standing interest in developing a
full and complete database, however, authors may also submit final
peer-reviewed manuscripts accepted before April 7, 2008, that arise
from NIH funds, if they have appropriate copyright permission or
authority.
D. Version Control
The NIH received comments with questions or concerns about the
version of the paper posted to PMC. Some commenters suggested that only
final, published versions of articles should be posted as they felt
final peer-reviewed manuscripts may contain scientific errors corrected
during the copy-editing process. A few commenters expressed concern
that the formatting processes that are part of PubMed Central may
change the meaning of the paper.
The NIH has been posting final peer-reviewed manuscripts on PMC for
years and found them to offer the same scientific information as the
final published article. The NIH obtains the permission of the author
before each author manuscript is posted to PMC. We ask authors to
review the specific document to be posted, and allow them to correct
any scientific issues during the approval process and afterwards. To
date, we are unaware of uncorrected errors in PubMed Central.
In response to questions about the version of a paper that may be
posted on PMC, the NIH issued FAQ D6 in May 2008. It explains that the
NIH Public Access Policy is based on a law (Division G, Title II,
Section 218 of Pub. L. 110-161) that requires investigators to submit
``their final, peer-reviewed manuscripts'' to PubMed Central. The NIH
will accept the final published article in lieu of the final peer-
reviewed manuscript, provided that the submitter has the right to
submit this version. Some journals post final published articles
directly to PMC. See https://publicaccess.nih.gov/submit_process_
journals.htm for more information.
Papers need to be converted into the PMC Archival format in order
to be posted. This process does not change the meaning or the content
of the paper. However, it does further the goals of the Public Access
Policy and is a fundamental feature of the PMC database. Once posted to
PubMed Central, results of NIH funded research become more prominent,
integrated, and accessible, making it easier for all scientists to
pursue NIH's research priority areas competitively. PubMed Central
materials are integrated with large NIH research databases such as
Genbank and PubChem, which helps accelerate scientific discovery.
Finally, the Policy allows the NIH to monitor, mine, and develop its
portfolio of taxpayer-funded research more effectively and archive its
results in perpetuity.
The NIH should provide guidance on copyright issues.
Some commenters requested explicit guidance on copyright issues.
The NIH provides an example in FAQ C3 (https://publicaccess.nih.gov/
FAQ.htm#c3), which states that ``* * * Individual copyright
arrangements can take many forms, and authors and their institutions
should continue to manage such arrangements as they have in the past.''
[[Page 7610]]
Institutions and investigators may wish to develop particular
copyright agreement terms in consultation with their own legal counsel
or other applicable official at their institution, as appropriate. As
an example, the kind of language that an author or institution might
add to a copyright agreement includes the following:
``Journal acknowledges that Author retains the right to provide a
copy of the final peer-reviewed manuscript to the NIH upon acceptance
for Journal publication, for public archiving in PubMed Central as soon
as possible but no later than 12 months after publication by Journal.''
7. Requests for Additional Information About the Policy and
Implementation Procedures.
A. NIH Should Disseminate Information About Publisher Support of the
Policy
Some commenters asked for a list of publishers that allow their
authors to comply with the policy. NIH has developed and maintains two
lists of publishers and journals. Hundreds of journals make the final
published version of every NIH-funded article publicly available in
PubMed Central within 12 months of publication without author
involvement. See https://publicaccess.nih.gov/submit_process_
journals.htm for a list of these journals. Some publishers will deposit
an individual final published article in PubMed Central upon author
request, and generally for a fee. See the list of publishers at https://
publicaccess.nih.gov/select_deposit_publishers.htm. All other
publisher policies and procedures require active author involvement to
finalize submission, as described in Methods C and D of the Policy Web
site (see https://publicaccess.nih.gov/submit_process.htm).
B. Frequently Asked Questions
Some commenters specifically highlighted the Frequently Asked
Questions as a helpful resource. A few mentioned the Public Access
Policy Web site in its entirety as helpful. The NIH also offers
additional resources to support training efforts, including complete
slide presentations that may be downloaded and adopted for stakeholder
use. These are available at https://publicaccess.nih.gov/
communications.htm.
8. Implementation Alternatives
A. Administrative Procedure Act
Some commenters felt the implementation of the Public Access Policy
was in violation of the Administrative Procedure Act. They claimed the
NIH should not have implemented the Policy without going through a
notice and comment rulemaking and that the January 11 Guide Notice
(https://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-033.html)
was issued inappropriately.
The NIH believes the initiation of notice and comment rulemaking to
implement the new statute is unwarranted and contrary to the interests
of science and the public health. The mandatory access requirement now
adopted in NIH Public Access Policy derives from Public Law 110-161,
Sec. 218, a Federal statute that was passed by Congress and signed by
the President of the United States. This statutory provision is a clear
and unambiguous directive to the NIH Director to require NIH grantees
to provide their manuscripts to PubMed Central after the date of
publication.
Where, as is true in this case, a statute clearly directs an agency
to execute a congressional objective, and Congress has not directed the
agency to promulgate implementing regulations, an agency's
interpretation or statement of policy or procedure regarding the
statute does not trigger a requirement for notice and comment
rulemaking. 5 U.S.C. 553(b)(3)(A); see also Shalala v. Guernsey Mem.
Hosp., 514 U.S. 87, 99 (1995); American Mining Congress v. Mine Safety
& Health Admin., 995 F.2d 1106, 1112 (D.C. Cir. 1993). Further, the
only significant difference between the new law and the NIH's former
voluntary public access policy is implementation of the legal directive
to require provision of the manuscripts; there is no ``gap'' left by
Congress that would require a rule to implement the statute. See
Chevron, U.S.A., Inc. v. NRDC, Inc., 467 U.S. 837, 843-44 (1984). The
mechanics of implementing the former policy were widely understood as
described in published agency policy and in widely accessible Internet
resources maintained by the NIH. Furthermore, the mechanics of
implementing the new statute are substantially the same as, and
consistent with, the NIH's earlier policy implementation. Agency
implementation of a plainly worded Congressional mandate--particularly
where consistent with established agency policy--does not require a
rulemaking proceeding. See, e.g., Gray Panthers Advocacy Cmte. v.
Sullivan, 936 F.2d 1284, 1291 (D.C. Cir. 1991). To the extent the NIH
has offered, and continues to offer, interpretative policy guidance or
procedural assistance with regard to the new law, such guidance is not
of free-standing legal effect but rather is intended to assist grantees
to comply with their statutory obligations. See American Mining
Congress, 995 F.2d at 1112. The impact of the mandatory submission
requirement arises from the statute, and rulemaking is not necessary to
implement this statutory requirement.
B. America Competes Act
Some commenters suggested the America Competes Act as an
alternative to the NIH's implementation. Relying on dissemination of
reports and abstracts as described in the America Competes Act is not
consistent with the Consolidated Appropriations Act of 2008.
C. A ``Dark Archive'' or Linking to Publisher or Other Web Sites
A few comments suggested that awardees should submit manuscripts to
the NIH for internal NIH reporting and portfolio management, and public
access could be provided by links to freely available materials on
publisher sites. Some comments suggested that the NIH only provide
public access via publisher sites, and not maintain an internal archive
at all. Many comments explicitly repudiated these ``dark archive'' or
linking approaches and argued that the policy should require deposit to
PubMed Central. One comment suggested that the Public Access Policy
mandate deposit to institutional archives (i.e., those maintained by
universities), and that these repositories could submit papers to
PubMed Central.
The Consolidated Appropriations Act of 2008 explicitly states that
papers should be submitted to and made publicly available on PubMed
Central and the NIH must follow this law. PubMed Central (PMC) is the
NIH National Library of Medicine's (NLM) digital repository of full-
text, peer-reviewed biomedical, behavioral, and clinical research
journals. NLM and its predecessor organizations have been archiving the
biomedical literature for over 150 years and are experienced in
maintaining a stable archive of scientific information. PMC is
currently used by approximately 400,000 users per day.
There are several critical advantages to the scientific community
for making papers publicly available on PMC. Once posted to PMC,
results of NIH-funded research become more prominent, integrated, and
accessible, making it easier for all scientists to pursue NIH's
research priority areas competitively. PMC materials are integrated
with large NIH research databases such as Genbank and PubChem, which
helps accelerate scientific discovery. Clinicians, patients, educators,
and students can better reap
[[Page 7611]]
the benefits of papers arising from NIH funding by accessing them on
PMC at no charge. Finally, the Policy allows NIH to monitor, mine, and
develop its portfolio of taxpayer-funded research more effectively, and
archive its results in perpetuity.
The Public Access Policy does not state that PMC will be the sole
repository for these manuscripts and publications. The NIH has always
pointed to journal and publisher sites from PMC and PubMed and will
continue to do so. See https://www.ncbi.nlm.nih.gov/projects/linkout/ for more information. Others may also post and/or archive papers
arising from NIH funds at other locations, subject to permission from
copyright holders, as appropriate.
9. Copyright Issues
A. Consistency With Copyright Law
The Consolidated Appropriations Act of 2008 requires that the NIH
implement the policy consistent with copyright law. Some commenters
suggested that that might not be possible.
The NIH disagrees with commenters' suggestions that it will be
difficult to implement the new statute in a manner that is consistent
with copyright law. To the contrary, the effect of the new statute is
merely that an author of a work that was funded by grants from the NIH
must retain, from the entire ``bundle of rights'' \3\ inherent in a
copyrightable work, a right to provide the author's manuscript to
PubMed Central for display on its Web site. The author (or his or her
employer) could, for instance, address this point in the agreement with
the publisher by a simple statement that reserves, on behalf of the
assignor, the right to provide the manuscript to PubMed Central for
display. Such a reservation of rights by the author is clearly
consistent with copyright law and the Consolidated Appropriations Act
of 2008.\4\
---------------------------------------------------------------------------
\3\ See 17 U.S.C. 106.
\4\ Copyright in a manuscript vests initially with the author
and remains with the author unless the rights are expressly
assigned. 17 U.S.C. 201(a). Of course, the author may be hired to
write the manuscript or may otherwise enter into an arrangement that
assigns the rights to an employer, making the employer the author
for purposes of the Copyright Act. 17 U.S.C. 201(b). Nevertheless,
the author owns all of the rights in the manuscript, and a potential
publisher owns no rights, unless and until they are conveyed by the
author to the publisher. A publisher that subsequently obtains
copyright to the work can continue to hold and enforce all of the
rights transferred by the author, subject to the principles of the
fair use doctrine, as are all copyrights. PubMed Central includes
many copyrighted works, and public use of a work on PubMed Central
is constrained by copyright, including the principles of fair use,
just as it would be if a member of the public viewed the publication
in a library, for example. Further, the public is alerted that the
works they are viewing may be subject to copyright, with the
following statement: ``This site also contains resources such as
PubMed Central, Bookshelf, OMIM, and PubChem which incorporate
material contributed or licensed by individuals, companies, or
organizations that may be protected by U.S. and foreign copyright
laws. All persons reproducing, redistributing, or making commercial
use of this information are expected to adhere to the terms and
conditions asserted by the copyright holder. Transmission or
reproduction of protected items beyond that allowed by fair use
(https://www.copyright.gov/fls/fl102.html) as defined in the
copyright laws requires the written permission of the copyright
owners.'' [https://www.ncbi.nlm.nih.gov/About/disclaimer.html]
---------------------------------------------------------------------------
U.S. Copyright law anticipates the transfer of ownership rights in
a copyright by agreement among parties or by operation of law (17
U.S.C. 201(d)). Publishers do not own any portion of a copyright in a
work that is not transferred to them by the author, or, if it is a work
for hire, under an employment agreement with the employing institution.
Similarly, the Federal Government, through OMB Circular A-110, grants
federally funded institutions the right to retain intangible property
(including copyright) as part of the terms and conditions of a Federal
grant. Congress could, if it wished, require grantees to assign all
rights to intangible property to the Federal funding agency, as indeed
was the case for patent rights prior to the Bayh-Dole Act of 1980.
However, in recognition of the public interest in having biomedical
scientific publications widely accessible, Congress has required only
that NIH-funded authors reserve the right to post works on PubMed
Central. As one among dozens of conditions imposed on a grantee by
Congress in return for taxpayer support of the grantee's work, the
reservation of this small sliver of the entire bundle of rights
inherent in the work is completely consistent with U.S. Copyright law.
B. Value of Publisher-Held Copyrights if Other Aspects of Copyright Are
Retained by Authors
A few comments indicated concern that posting the final peer-
reviewed manuscript to PubMed Central undermines the value of all other
aspects of copyright that a Publisher may have obtained under the
Policy.
As described above, it is acceptable from a copyright perspective
for investigators to ensure their papers can be posted to PubMed
Central. However, the NIH Public Access Policy applies to awardees, not
publishers. The NIH implemented the Public Access Policy prospectively
to ensure that publishers have the ability to refuse to publish any
paper they wish, for any reason they wish, including not obtaining all
the rights they may prefer from authors of papers arising from NIH
funds. The 12-month delay period and the ability of NIH awardees to
cover publication-related costs from their awards are important aspects
of the Policy created specifically to address concerns of some
publishers and ensure their interests are protected.
These comments concerning loss of value of the copyrighted work
were not supported by data and run contrary to NIH's experience. The
voluntary support of hundreds of journals to collect papers under the
Policy is, perhaps, a reflection of publisher protections in the Public
Access Policy. A significant number of journals support their authors
by volunteering to submit manuscripts, and many more go beyond the
policy by submitting final published articles. Hundreds even deposit
final published articles that do not arise from NIH funds. Many of
these journals also permit their papers to be posted to PubMed Central
before the 12-month maximum delay period. The NIH appreciates the
efforts of all these journals to support the Policy.
C. Section 201(E) of the Copyright Act
One comment raised a concern that Section 201(e) of the Copyright
Act prohibits a requirement for NIH awardees to retain a right to
deposit in PMC. Section 201(e) of the Copyright Act states that when an
individual author's ownership of a copyright has not previously been
transferred voluntarily by that individual author, no action by any
governmental body purporting to seize copyright shall take effect.
Section 201(e) does not apply to the PMC situation for many
reasons. First, the works at issue here are for the most part works in
which the author has already expressly agreed how copyright will be
handled through the employment agreement with their employing
institution (see 201(b) works made for hire). Second, the employing
institution will have previously accepted, as a term and condition of
the grant, the obligation to submit a work created under the grant to
PMC. Third, Congress did not require an involuntary transfer of rights,
or otherwise ``seize'' rights. Rather, it required submission of the
manuscript to PMC. One way of complying with this requirement would be
for the author to retain the right to post, rather than transfer that
right to a third party. Such retention by the author does not
constitute a seizure or involuntary transfer of rights. Copyrighted
material on PMC remains
[[Page 7612]]
fully subject to copyright, and copyright owners may fully enforce
their rights. Fourth, to the extent that the PMC requirement can be
read as a Government-retained interest, Congress often requires funding
agencies to retain certain rights in the public interest in tangible
and intangible property first produced with public funds. To read the
patent or copyright laws as preventing such action would overturn many
long-standing provisions of OMB Circular A-110 as well as the Federal
Acquisition Regulation (F.A.R.) (e.g., rights in data first produced in
its procurement contracts, rights in inventions, rights in computer
software).
D. International Copyright Issues
A few comments suggested that copyright concerns stem from making
materials available on the Internet, and therefore internationally
available. The NIH appreciates that the scientific community is truly
global and interchange among scientists worldwide is essential for
professional and scientific advancement. The Polic