COVID-19 Prioritized Examination Pilot Program, 28932-28935 [2020-10372]
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28932
Federal Register / Vol. 85, No. 94 / Thursday, May 14, 2020 / Notices
Notification Regarding Administrative
Protective Orders
This notice serves as the only
reminder to parties subject to
administrative protective order (APO) of
their responsibility concerning the
disposition of proprietary information
disclosed under APO in accordance
with 19 CFR 351.305(a)(3). Timely
written notification of the return or
destruction of APO materials or
conversion to judicial protective order is
hereby requested. Failure to comply
with the regulations and the terms of an
APO is a sanctionable violation. Note
that Commerce has temporarily
modified certain of its requirements for
serving documents containing business
proprietary information, until May 19,
2020, unless extended.11
This notice is published in
accordance with sections 751(a)(1) and
777(i)(1) of the Act, and 19 CFR
351.213(d)(4).
Dated: May 8, 2020.
James Maeder,
Deputy Assistant Secretary for Antidumping
and Countervailing Duty Operations.
[FR Doc. 2020–10350 Filed 5–13–20; 8:45 am]
BILLING CODE 3510–DS–P
DEPARTMENT OF COMMERCE
National Institute of Standards and
Technology
Open Meeting of the Information
Security and Privacy Advisory Board
National Institute of Standards
and Technology, Department of
Commerce.
ACTION: Notice of open meeting.
AGENCY:
The Information Security and
Privacy Advisory Board (ISPAB) will
meet Wednesday, June 24, 2020 from
9:00 a.m. until 5:00 p.m., Eastern Time,
and Thursday, June 25, 2020 from 9:00
a.m. until 4:30 p.m., Eastern Time. All
sessions will be open to the public.
DATES: The meeting will be held on
Wednesday, June 24, 2020, from 9:00
a.m. until 5:00 p.m., Eastern Time, and
Thursday, June 25, 2020, from 9:00 a.m.
until 4:30 p.m., Eastern Time.
ADDRESSES: The meeting will be a
virtual meeting via webinar. Please note
admittance instructions under the
SUPPLEMENTARY INFORMATION section of
this notice.
FOR FURTHER INFORMATION CONTACT: Jeff
Brewer, Information Technology
Laboratory, National Institute of
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SUMMARY:
11 See Temporary Rule Modifying AD/CVD
Service Requirements Due to COVID–19, 85 FR
17006 (March 26, 2020).
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Standards and Technology, Telephone:
(301) 975–2489, Email address:
jeffrey.brewer@nist.gov.
SUPPLEMENTARY INFORMATION: Pursuant
to the Federal Advisory Committee Act,
as amended, 5 U.S.C. App., notice is
hereby given that the ISPAB will hold
an open meeting Wednesday, June 24,
2020 from 9:00 a.m. until 5:00 p.m.,
Eastern Time, and Thursday, June 25,
2020 from 9:00 a.m. until 4:30 p.m.
Eastern Time. All sessions will be open
to the public. The ISPAB is authorized
by 15 U.S.C. 278g–4, as amended, and
advises the National Institute of
Standards and Technology (NIST), the
Secretary of Homeland Security, and the
Director of the Office of Management
and Budget (OMB) on information
security and privacy issues pertaining to
Federal government information
systems, including through review of
proposed standards and guidelines
developed by NIST. Details regarding
the ISPAB’s activities are available at
https://csrc.nist.gov/projects/ispab.
The agenda is expected to include the
following items:
—Discussion of the United States
Methods of Product Testing and
Standards Conformance,
—Presentation from the United States
Government Testing Programs,
—Discussion of International Testing
requirements and conformance
regimes,
—Discussion of Executive Order
13905—Strengthening National
Resilience Through Use of
Positioning, Navigation, and Timing
(PNT) Services,
—Discussion on telework cybersecurity
and privacy, and potential lessons
learned
Note that agenda items may change
without notice. The final agenda will be
posted on the ISPAB event page at:
https://cms.csrc.nist.gov/Events/2020/
ispab-june-meeting.
Public Participation: Written
questions or comments from the public
are invited and may be submitted
electronically by email to Jeff Brewer at
the contact information indicated in the
FOR FURTHER INFORMATION CONTACT
section of this notice by 5 p.m. June 22,
2020.
The ISPAB agenda will include a
period, not to exceed thirty minutes, for
submitted questions or comments from
the public (Wednesday, June 24, 2020,
between 4:30 p.m. and 5:00 p.m.).
Submitted questions or comments from
the public will be selected on a firstcome, first-served basis and limited to
five minutes per person.
Members of the public who wish to
expand upon their submitted
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statements, those who had wished to
submit a question or comment but could
not be accommodated on the agenda,
and those who were unable to attend the
meeting via webinar are invited to
submit written statements. In addition,
written statements are invited and may
be submitted to the ISPAB at any time.
All written statements should be
directed to the ISPAB Secretariat,
Information Technology Laboratory by
email to: jeffrey.brewer@nist.gov.
Admittance Instructions: All
participants will be attending via
webinar and must register on ISPAB’s
event page at: https://cms.csrc.nist.gov/
Events/2020/ispab-june-meeting by 5
p.m. Eastern Time, June 22, 2020.
Kevin A. Kimball,
Chief of Staff.
[FR Doc. 2020–10375 Filed 5–13–20; 8:45 am]
BILLING CODE 3510–13–P
DEPARTMENT OF COMMERCE
Patent and Trademark Office
[Docket No.: PTO–P–2020–0026]
COVID–19 Prioritized Examination Pilot
Program
United States Patent and
Trademark Office, Department of
Commerce.
ACTION: Notice.
AGENCY:
The United States Patent and
Trademark Office (USPTO or Office) is
implementing a pilot program to
provide prioritized examination of
certain patent applications. To qualify,
the claim(s) of an application must
cover a product or process related to
COVID–19, and such product or process
must be subject to an applicable FDA
approval for COVID–19 use.
Under this pilot program, the USPTO
will grant qualified requests for
prioritized examination without
payment of certain fees associated with
prioritized examination for applicants
that qualify for small or micro entity
status. The goal of prioritized
examination is to provide a final
disposition within 12 months, on
average, from the date the prioritized
status has been granted. Furthermore,
the USPTO believes it can achieve final
disposition in six months if applicants
provide more timely responses to
notices and actions from the USPTO, as
compared to those required by
prioritized examination. This notice
outlines the conditions, eligibility
requirements, and guidelines of the
pilot program.
SUMMARY:
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Federal Register / Vol. 85, No. 94 / Thursday, May 14, 2020 / Notices
Comments must be received by
July 13, 2020 to ensure consideration.
Pilot Duration: The COVID–19
Prioritized Examination Pilot Program
will accept requests for prioritized
examination beginning July 13, 2020
until such time as the USPTO has
accepted a total of 500 requests. The
USPTO may extend the pilot program
(with or without modifications) or
terminate it depending on the workload
and resources needed to administer the
program, feedback from the public, and
the effectiveness of the program. If the
pilot program is extended or terminated,
the USPTO will notify the public.
ADDRESSES: Comments should be sent
by email addressed to
Covid19PrioritizedExamPilot@
uspto.gov. If submission of comments by
email is not feasible due to, e.g., a lack
of access to a computer and/or the
internet, please contact the USPTO for
special instructions using the contact
information provided in the FOR
FURTHER INFORMATION CONTACT section of
this notice.
Comments will be available for
viewing via the USPTO’s website
(https://www.uspto.gov). Because the
comments will be made available for
public viewing, information the
submitter does not desire to make
public, such as an address or phone
number, should not be included in the
comments.
FOR FURTHER INFORMATION CONTACT:
Robert A. Clarke, Editor of the Manual
of Patent Examining Procedure (MPEP)
(telephone at 571–272–7735; email at
robert.clarke@uspto.gov).
SUPPLEMENTARY INFORMATION: New
patent applications are normally taken
up for examination in the order of their
U.S. filing dates. See section 708 of the
MPEP (9th ed., Rev. 08.2017, 2018). The
USPTO has procedures under which an
application will be advanced out of turn
(accorded special status) for
examination if the applicant files a
petition to make special under 37 CFR
1.102(c) and (d) with the appropriate
showing. See 37 CFR 1.102(c) and (d)
and MPEP 708.02 and 708.02(a).
In addition, an application can be
advanced out of turn (accorded special
status) for examination if the applicant
files a grantable request for prioritized
examination under 37 CFR 1.102(e).
Section 11(h) of the Leahy-Smith
America Invents Act, Public Law 112–
29, 125 Stat. 284 (2011), effective
September 26, 2011, provides for
prioritized examination whereby an
applicant may request prioritized
examination upon payment of
appropriate fees and compliance with
certain requirements. See MPEP
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708.02(b). 35 U.S.C. 2(b)(2)(G)
authorizes the USPTO to provide for
prioritization of examination of
applications for products, processes, or
technologies that are important to the
national economy or national
competitiveness without requiring the
prioritized examination fee.
In an extraordinary situation, 37 CFR
1.183 permits the USPTO to suspend or
waive sua sponte any requirement of its
regulations that is not a requirement of
the patent statutes. The USPTO
considers the effects of the COVID–19
outbreak that began in approximately
January 2020 to be an ‘‘extraordinary
situation’’ within the meaning of 37 CFR
1.183 for affected patent applicants and
innovators. Consistent with this
determination and the provisions of 35
U.S.C. 2(b)(2)(G), the USPTO has
decided to implement a pilot program to
provide prioritized examination without
payment of the additional fees for
prioritized examination for certain
applications that claim products or
processes that are subject to an
applicable FDA approval for COVID–19
use. Such approvals may include, but
are not limited to, an Investigational
New Drug (IND) application, an
Investigational Device Exemption (IDE),
a New Drug Application (NDA), a
Biologics License Application (BLA), a
Premarket Approval (PMA), or an
Emergency Use Authorization (EUA).
Information on INDs, IDEs, NDAs,
BLAs, PMAs, and EUAs may be
obtained at www.fda.gov. To focus the
USPTO’s resources on those applicants
that may be more resource constrained,
the pilot is limited to applicants that
qualify for either small or micro entity
status. The USPTO will periodically
evaluate the pilot program to determine
whether and to what extent its coverage
should be expanded or limited.
The USPTO currently provides for
prioritized examination of utility and
plant original applications if certain
requirements are met. See 37 CFR
1.102(e) and MPEP 708.02(b). Upon
filing a request for prioritized
examination, an applicant must pay
certain fees, including a prioritized
examination fee set forth in 37 CFR
1.17(c) and a processing fee set forth in
37 CFR 1.17(i)(1). The requirement to
pay these two fees will be waived under
this pilot program if the requirements
are met. The remaining fees listed in 37
CFR 1.102(e) and MPEP 708.02(b),
subsection I. A. 2., that are not currently
set to $0 must be paid by all applicants,
and the requirement to pay those fees by
the time the request for prioritized
examination is made is not waived
under this pilot program.
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Part I. Requirements To Participate
(1) The request for prioritized
examination under the pilot program
must be made:
(a) With the filing of a non-continuing
original utility or plant nonprovisional
application;
(b) with the filing of an original utility
or plant nonprovisional application
claiming the benefit of an earlier filing
date under 35 U.S.C. 120, 121, or 365(c)
of one prior nonprovisional application
or one prior international application
designating the United States; or
(c) with or after the filing of a request
for continued examination (RCE) of
such plant or utility application or of a
national stage of an international
application. Consistent with 37 CFR
1.102(e)(2), only a single request for
prioritized examination filed with or
after filing an RCE may be granted in an
application.
The pilot program is reserved for the
above nonprovisional applications. Any
application that claims the benefit of the
filing date of two or more prior filed
nonprovisional U.S. applications or
international applications designating
the United States under 35 U.S.C. 120,
121, or 365(c) is not eligible for
participation under the pilot program,
but the applicant may request
prioritized examination under 37 CFR
1.102(e). Claiming the benefit under 35
U.S.C. 119(e) of one or more prior
provisional applications or claiming a
right of foreign priority under 35 U.S.C.
119(a)–(d) or (f) to one or more foreign
applications will not cause a
nonprovisional application to be
ineligible for the pilot program.
The USPTO encourages the use of
form PTO/SB/450, titled ‘‘Certification
and Request for COVID–19 Prioritized
Examination Pilot Program under 37
CFR 1.102(e),’’ to make the request for
prioritized examination under the pilot.
Form PTO/SB/450 is available at
https://www.uspto.gov/patent/forms/
forms-patent-applications-filed-or-afterseptember-16-2012. Form PTO/SB/450
contains the necessary certifications for
qualification to participate in the pilot.
Use of form PTO/SB/450 will also
enable the USPTO to quickly identify
and timely process the request.
(2) The applicant must certify that at
least one of the pending claims covers
a product or process related to COVID–
19 and that such product or process is
subject to an applicable FDA approval
for COVID–19 use. Form PTO/SB/450
contains this certification.
(3) The request must include a
certification that the applicant qualifies
for either small entity (37 CFR 1.27) or
micro entity (37 CFR 1.29) status when
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the request is made. Form PTO/SB/450
contains this certification.
(4) The request must include an
executed application data sheet meeting
the conditions specified in 37 CFR
1.53(f)(3)(i).
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Part II. Internal Processing of the
Request Under the Pilot Program
Requests complying with the four
requirements above will be further
reviewed to determine if the other
requirements for prioritized
examination are met, e.g., the
requirements of 37 CFR 1.102(e) other
than payment of the fees set forth in 37
CFR 1.17(c) and 1.17(i)(1). These
requirements include: Filing the
application and request for prioritized
examination under the pilot program via
the USPTO’s patent electronic filing
systems (EFS-Web or Patent Center) if
the application is a utility application;
presenting no more than four
independent claims and 30 total claims,
and no multiple dependent claims; and
paying the other required fees (e.g., the
basic filing fee, search fee, and
examination fee). In addition, obtaining
an extension of time to a notice before
the request has been acted upon will
result in the request being denied. See
MPEP 708.02(b), subsection I, for a
discussion of the requirements.
Part III. Office Actions and Replies
Under the Pilot Program
The time periods set for reply in
Office actions for applications
undergoing prioritized examination
under the pilot program will be the
same as those for other applications
undergoing prioritized examination and
are set forth in MPEP 710.02(b). If an
applicant files a petition for an
extension of time to file a reply or a
request for suspension of action, the
petition or request will be acted upon,
but the prioritized examination of the
application under the pilot program will
be terminated, as is the case with other
applications undergoing prioritized
examination. In addition, in order to
maintain special status, filing an
amendment to the application that
results in more than four independent
claims, more than 30 total claims, or a
multiple dependent claim will
terminate the prioritized examination,
as is the case with other applications
undergoing prioritized examination.
Upon termination of prioritized
examination, the application will be
removed from the examiner’s special
docket and placed on the examiner’s
regular docket in accordance with its
stage of prosecution, as is the case with
other applications undergoing
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A reply to an Office action must be
fully responsive to the rejections,
objections, and requirements made by
the examiner. Any amendment filed in
reply to a non-final Office action will be
treated as not fully responsive if it
attempts to: (1) Add claims that would
result in more than four independent
claims or more than 30 total claims
pending in the application; or (2) add
any multiple dependent claim. If a reply
to a non-final Office action is not fully
responsive because it does not comply
with the pilot program requirements but
is a bona fide attempt to advance the
application to final action, the examiner
may, at his or her discretion, provide
one month or 30 days, whichever is
longer, for the applicant to supply a
fully responsive reply, in which case
prioritized examination would not be
terminated. Submission of a petition for
extension of time under 37 CFR 1.136(a)
to the notice of nonresponsive
amendment will result in termination of
special status. Any further
nonresponsive amendment will not be
treated as bona fide, and the time period
set in the prior notice will continue to
run.
Part IV. After-Final and Appeal
Procedures
The mailing of a final Office action or
the filing of a Notice of Appeal,
whichever is earlier, is a final
disposition for purposes of the 12month goal for the pilot program.
During the appeal process, the
application will be treated in
accordance with the normal appeal
procedure (see MPEP chapter 1200).
Any amendment, affidavit, or other
evidence submitted after a final Office
action and prior to appeal must comply
with 37 CFR 1.116. The filing of an RCE
for an application in the pilot program
is a final disposition for purposes of the
12-month goal for the program. The
application will not retain its special
status after the filing of a proper RCE.
Part V. Proceedings Outside the Normal
Examination Process
If an application becomes involved in
proceedings outside the normal
examination process (e.g., a secrecy
order or petitions under 37 CFR 1.181–
1.183), the USPTO will place the
application in special status under the
pilot program before and after such
proceedings. During those proceedings,
however, the application will not be
under special status. For example, while
under a secrecy order, the application
will be treated in accordance with the
normal secrecy order procedures and
will not be in special status under the
pilot program. Once the proceeding
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outside the normal examination process
is completed, the application will
continue in special status until it
reaches a final disposition, which may
occur later than 12 months from the
grant of special status under the pilot
program.
Part VI. First Action Interview (FAI)
Pilot Program Is Not Available
Applications accepted into the FAI
Pilot Program are not eligible for this
pilot program. In addition, applications
accepted into this pilot program will not
be eligible to participate in the FAI Pilot
Program. However, standard interview
practices and procedures applicable to
regular ex parte prosecution will still be
available. See MPEP 713.02. For more
information about the FAI Pilot
Program, please visit https://
www.uspto.gov/patent/initiatives/firstaction-interview/full-first-actioninterview-pilot-program.
Part VII. Actions Resulting in
Termination From the Pilot Program
There is no provision for withdrawal
from special status under the pilot
program. However, the filing of a
petition for any extension of time under
37 CFR 1.136(a) will result in the
termination of special status under the
pilot program. Presenting more than one
benefit claim to previously filed
nonprovisional U.S. applications or
international applications designating
the United States under 35 U.S.C. 120,
121, or 365(c) will also result in the
termination of special status under the
pilot program.
An applicant may abandon the
application that has been granted
special status under the pilot program in
favor of a continuing application.
However, a continuing application will
not automatically be given prioritized
examination status based on the request
filed in the parent application. Each
application (including each continuing
application) must, on its own, meet all
requirements for prioritized
examination under the pilot program.
Part VIII. Twelve-Month Goal
The objective of the pilot program is
to complete, on average, the
examination of an application within 12
months of special status being granted
(i.e., within 12 months from the mailing
date of the decision granting the petition
to make special). The 12-month goal is
successfully achieved when one of the
following final dispositions occurs
within 12 months from the grant of
special status under the pilot program:
(1) The mailing of a notice of allowance;
(2) the mailing of a final Office action;
(3) the filing of an RCE; (4) the
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abandonment of the application; or (5)
the filing of a Notice of Appeal. The
final disposition of an application,
however, may occur later than the 12month time frame in certain situations
(e.g., when the applicant filed a petition
under 37 CFR 1.181). In any event,
however, the 12-month time frame is a
goal. Any failure to meet the 12-month
goal, or other issues related to this goal
that arise, are neither petitionable nor
appealable matters.
Applicants may shorten the overall
pendency of an application in the pilot
program by replying to Office actions
and notices earlier than required by the
USPTO. For example, the USPTO will
endeavor to reduce pendency, from
approval of the request for prioritized
examination to final disposition, to six
months if all replies occur within 30
days of a notice by the USPTO. This
goal depends on additional factors,
including the demands placed on
specific examiners by multiple copending applications under the pilot
program. Current statistics for
prioritized examination are available at
https://www.uspto.gov/corda/
dashboards/patents/main.dashxml?
CTNAVID=1007.
Andrei Iancu,
Under Secretary of Commerce for Intellectual
Property and Director of the United States
Patent and Trademark Office.
[FR Doc. 2020–10372 Filed 5–13–20; 8:45 am]
BILLING CODE 3510–16–P
DEPARTMENT OF DEFENSE
Department of the Air Force
[Docket ID: USAF–2020–HQ–0006]
Proposed Collection; Comment
Request
AGENCY:
Department of the Air Force,
DoD.
ACTION:
Information collection notice.
In compliance with the
Paperwork Reduction Act of 1995, the
Department of the Air Force announces
a proposed public information
collection and seeks public comment on
the provisions thereof. Comments are
invited on: Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; the accuracy of the
agency’s estimate of the burden of the
proposed information collection; ways
to enhance the quality, utility, and
clarity of the information to be
collected; and ways to minimize the
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SUMMARY:
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burden of the information collection on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
DATES: Consideration will be given to all
comments received by July 13, 2020.
ADDRESSES: You may submit comments,
identified by docket number and title,
by any of the following methods:
Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Mail: DoD cannot receive written
comments at this time due to the
COVID–19 pandemic. Comments should
be sent electronically to the docket
listed above.
Instructions: All submissions received
must include the agency name, docket
number and title for this Federal
Register document. The general policy
for comments and other submissions
from members of the public is to make
these submissions available for public
viewing on the internet at https://
www.regulations.gov as they are
received without change, including any
personal identifiers or contact
information.
FOR FURTHER INFORMATION CONTACT: To
request more information on this
proposed information collection or to
obtain a copy of the proposal and
associated collection instruments,
please write to CMOS, 200 East Moore
Dr., Maxwell AFB Gunter Annex, AL
36114–3004, ATTN: Daniel J. Mangum,
(334) 416–4679.
SUPPLEMENTARY INFORMATION:
Title; Associated Form; and OMB
Number: Cargo Movement Operations
System (CMOS); OMB Control Number
0701–CMOS.
Needs and Uses: CMOS is used by the
DoD to plan, manage, and execute the
movement of cargo and personnel. In
addition to the deployment of active
military personnel, the passenger
manifest capability supports military
retirees and military family members
traveling on a ‘‘Space A CAT VI’’ basis.
Those passengers are considered to be
‘‘general public.’’ The data required for
a passenger manifest includes PII, such
as a Passport Number, and is deemed to
be a ‘‘Collection.’’ This ‘‘general public’’
data is collected when passengers are at
the Air Terminal; no solicitation is
involved.
Affected Public: Individuals and
Household.
Annual Burden Hours: 18.
Number of Respondents: 180.
Responses per Respondent: 1.
Annual Responses: 180.
Average Burden per Response: 0.1
hour.
Frequency: Approximately 180 times
per year.
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28935
This passenger data is collected only
on an as-needed basis when the
passengers request the Space A travel,
and is collected only at the Air
Terminal. CMOS does not seek out these
respondents and does not in any way
solicit their participation. There are no
paper forms for information requests
sent to the travelers for them to return.
The sole purpose of this data is to
provide a complete manifest of the
passengers onboard the military flight. It
is not used for any other reporting or
statistical purposes.
Dated: May 11, 2020.
Aaron T. Siegel,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. 2020–10342 Filed 5–13–20; 8:45 am]
BILLING CODE 5001–06–P
DEPARTMENT OF DEFENSE
Department of the Air Force
[Docket ID: USAF–2020–HQ–0005]
Proposed Collection, Comment
Request
Headquarters Air Force
Personnel Center/Airman and Family
Sustainment Branch, Department of
Defense.
ACTION: Information collection notice.
AGENCY:
In compliance with the
Paperwork Reduction Act of 1995, the
Airman and Family Sustainment
Branch, Headquarters Air Force
Personnel Center, announces the
proposed reinstatement of a public
information collection and seeks public
comment on the provisions thereof.
Comments are invited on: Whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information shall have
practical utility; the accuracy of the
agency’s estimate of the burden of the
proposed information collection; ways
to enhance the quality, utility, and
clarity of the information to be
collected; and ways to minimize the
burden of the information collection on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
DATES: Consideration will be given to all
comments received by July 13, 2020.
ADDRESSES: You may submit comments,
identified by docket number and title,
by any of the following methods:
Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
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SUMMARY:
E:\FR\FM\14MYN1.SGM
14MYN1
Agencies
[Federal Register Volume 85, Number 94 (Thursday, May 14, 2020)]
[Notices]
[Pages 28932-28935]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-10372]
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DEPARTMENT OF COMMERCE
Patent and Trademark Office
[Docket No.: PTO-P-2020-0026]
COVID-19 Prioritized Examination Pilot Program
AGENCY: United States Patent and Trademark Office, Department of
Commerce.
ACTION: Notice.
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SUMMARY: The United States Patent and Trademark Office (USPTO or
Office) is implementing a pilot program to provide prioritized
examination of certain patent applications. To qualify, the claim(s) of
an application must cover a product or process related to COVID-19, and
such product or process must be subject to an applicable FDA approval
for COVID-19 use.
Under this pilot program, the USPTO will grant qualified requests
for prioritized examination without payment of certain fees associated
with prioritized examination for applicants that qualify for small or
micro entity status. The goal of prioritized examination is to provide
a final disposition within 12 months, on average, from the date the
prioritized status has been granted. Furthermore, the USPTO believes it
can achieve final disposition in six months if applicants provide more
timely responses to notices and actions from the USPTO, as compared to
those required by prioritized examination. This notice outlines the
conditions, eligibility requirements, and guidelines of the pilot
program.
[[Page 28933]]
DATES: Comments must be received by July 13, 2020 to ensure
consideration.
Pilot Duration: The COVID-19 Prioritized Examination Pilot Program
will accept requests for prioritized examination beginning July 13,
2020 until such time as the USPTO has accepted a total of 500 requests.
The USPTO may extend the pilot program (with or without modifications)
or terminate it depending on the workload and resources needed to
administer the program, feedback from the public, and the effectiveness
of the program. If the pilot program is extended or terminated, the
USPTO will notify the public.
ADDRESSES: Comments should be sent by email addressed to
[email protected]. If submission of comments by
email is not feasible due to, e.g., a lack of access to a computer and/
or the internet, please contact the USPTO for special instructions
using the contact information provided in the FOR FURTHER INFORMATION
CONTACT section of this notice.
Comments will be available for viewing via the USPTO's website
(https://www.uspto.gov). Because the comments will be made available
for public viewing, information the submitter does not desire to make
public, such as an address or phone number, should not be included in
the comments.
FOR FURTHER INFORMATION CONTACT: Robert A. Clarke, Editor of the Manual
of Patent Examining Procedure (MPEP) (telephone at 571-272-7735; email
at [email protected]).
SUPPLEMENTARY INFORMATION: New patent applications are normally taken
up for examination in the order of their U.S. filing dates. See section
708 of the MPEP (9th ed., Rev. 08.2017, 2018). The USPTO has procedures
under which an application will be advanced out of turn (accorded
special status) for examination if the applicant files a petition to
make special under 37 CFR 1.102(c) and (d) with the appropriate
showing. See 37 CFR 1.102(c) and (d) and MPEP 708.02 and 708.02(a).
In addition, an application can be advanced out of turn (accorded
special status) for examination if the applicant files a grantable
request for prioritized examination under 37 CFR 1.102(e). Section
11(h) of the Leahy-Smith America Invents Act, Public Law 112-29, 125
Stat. 284 (2011), effective September 26, 2011, provides for
prioritized examination whereby an applicant may request prioritized
examination upon payment of appropriate fees and compliance with
certain requirements. See MPEP 708.02(b). 35 U.S.C. 2(b)(2)(G)
authorizes the USPTO to provide for prioritization of examination of
applications for products, processes, or technologies that are
important to the national economy or national competitiveness without
requiring the prioritized examination fee.
In an extraordinary situation, 37 CFR 1.183 permits the USPTO to
suspend or waive sua sponte any requirement of its regulations that is
not a requirement of the patent statutes. The USPTO considers the
effects of the COVID-19 outbreak that began in approximately January
2020 to be an ``extraordinary situation'' within the meaning of 37 CFR
1.183 for affected patent applicants and innovators. Consistent with
this determination and the provisions of 35 U.S.C. 2(b)(2)(G), the
USPTO has decided to implement a pilot program to provide prioritized
examination without payment of the additional fees for prioritized
examination for certain applications that claim products or processes
that are subject to an applicable FDA approval for COVID-19 use. Such
approvals may include, but are not limited to, an Investigational New
Drug (IND) application, an Investigational Device Exemption (IDE), a
New Drug Application (NDA), a Biologics License Application (BLA), a
Premarket Approval (PMA), or an Emergency Use Authorization (EUA).
Information on INDs, IDEs, NDAs, BLAs, PMAs, and EUAs may be obtained
at www.fda.gov. To focus the USPTO's resources on those applicants that
may be more resource constrained, the pilot is limited to applicants
that qualify for either small or micro entity status. The USPTO will
periodically evaluate the pilot program to determine whether and to
what extent its coverage should be expanded or limited.
The USPTO currently provides for prioritized examination of utility
and plant original applications if certain requirements are met. See 37
CFR 1.102(e) and MPEP 708.02(b). Upon filing a request for prioritized
examination, an applicant must pay certain fees, including a
prioritized examination fee set forth in 37 CFR 1.17(c) and a
processing fee set forth in 37 CFR 1.17(i)(1). The requirement to pay
these two fees will be waived under this pilot program if the
requirements are met. The remaining fees listed in 37 CFR 1.102(e) and
MPEP 708.02(b), subsection I. A. 2., that are not currently set to $0
must be paid by all applicants, and the requirement to pay those fees
by the time the request for prioritized examination is made is not
waived under this pilot program.
Part I. Requirements To Participate
(1) The request for prioritized examination under the pilot program
must be made:
(a) With the filing of a non-continuing original utility or plant
nonprovisional application;
(b) with the filing of an original utility or plant nonprovisional
application claiming the benefit of an earlier filing date under 35
U.S.C. 120, 121, or 365(c) of one prior nonprovisional application or
one prior international application designating the United States; or
(c) with or after the filing of a request for continued examination
(RCE) of such plant or utility application or of a national stage of an
international application. Consistent with 37 CFR 1.102(e)(2), only a
single request for prioritized examination filed with or after filing
an RCE may be granted in an application.
The pilot program is reserved for the above nonprovisional
applications. Any application that claims the benefit of the filing
date of two or more prior filed nonprovisional U.S. applications or
international applications designating the United States under 35
U.S.C. 120, 121, or 365(c) is not eligible for participation under the
pilot program, but the applicant may request prioritized examination
under 37 CFR 1.102(e). Claiming the benefit under 35 U.S.C. 119(e) of
one or more prior provisional applications or claiming a right of
foreign priority under 35 U.S.C. 119(a)-(d) or (f) to one or more
foreign applications will not cause a nonprovisional application to be
ineligible for the pilot program.
The USPTO encourages the use of form PTO/SB/450, titled
``Certification and Request for COVID-19 Prioritized Examination Pilot
Program under 37 CFR 1.102(e),'' to make the request for prioritized
examination under the pilot. Form PTO/SB/450 is available at https://www.uspto.gov/patent/forms/forms-patent-applications-filed-or-after-september-16-2012. Form PTO/SB/450 contains the necessary
certifications for qualification to participate in the pilot. Use of
form PTO/SB/450 will also enable the USPTO to quickly identify and
timely process the request.
(2) The applicant must certify that at least one of the pending
claims covers a product or process related to COVID-19 and that such
product or process is subject to an applicable FDA approval for COVID-
19 use. Form PTO/SB/450 contains this certification.
(3) The request must include a certification that the applicant
qualifies for either small entity (37 CFR 1.27) or micro entity (37 CFR
1.29) status when
[[Page 28934]]
the request is made. Form PTO/SB/450 contains this certification.
(4) The request must include an executed application data sheet
meeting the conditions specified in 37 CFR 1.53(f)(3)(i).
Part II. Internal Processing of the Request Under the Pilot Program
Requests complying with the four requirements above will be further
reviewed to determine if the other requirements for prioritized
examination are met, e.g., the requirements of 37 CFR 1.102(e) other
than payment of the fees set forth in 37 CFR 1.17(c) and 1.17(i)(1).
These requirements include: Filing the application and request for
prioritized examination under the pilot program via the USPTO's patent
electronic filing systems (EFS-Web or Patent Center) if the application
is a utility application; presenting no more than four independent
claims and 30 total claims, and no multiple dependent claims; and
paying the other required fees (e.g., the basic filing fee, search fee,
and examination fee). In addition, obtaining an extension of time to a
notice before the request has been acted upon will result in the
request being denied. See MPEP 708.02(b), subsection I, for a
discussion of the requirements.
Part III. Office Actions and Replies Under the Pilot Program
The time periods set for reply in Office actions for applications
undergoing prioritized examination under the pilot program will be the
same as those for other applications undergoing prioritized examination
and are set forth in MPEP 710.02(b). If an applicant files a petition
for an extension of time to file a reply or a request for suspension of
action, the petition or request will be acted upon, but the prioritized
examination of the application under the pilot program will be
terminated, as is the case with other applications undergoing
prioritized examination. In addition, in order to maintain special
status, filing an amendment to the application that results in more
than four independent claims, more than 30 total claims, or a multiple
dependent claim will terminate the prioritized examination, as is the
case with other applications undergoing prioritized examination. Upon
termination of prioritized examination, the application will be removed
from the examiner's special docket and placed on the examiner's regular
docket in accordance with its stage of prosecution, as is the case with
other applications undergoing prioritized examination.
A reply to an Office action must be fully responsive to the
rejections, objections, and requirements made by the examiner. Any
amendment filed in reply to a non-final Office action will be treated
as not fully responsive if it attempts to: (1) Add claims that would
result in more than four independent claims or more than 30 total
claims pending in the application; or (2) add any multiple dependent
claim. If a reply to a non-final Office action is not fully responsive
because it does not comply with the pilot program requirements but is a
bona fide attempt to advance the application to final action, the
examiner may, at his or her discretion, provide one month or 30 days,
whichever is longer, for the applicant to supply a fully responsive
reply, in which case prioritized examination would not be terminated.
Submission of a petition for extension of time under 37 CFR 1.136(a) to
the notice of nonresponsive amendment will result in termination of
special status. Any further nonresponsive amendment will not be treated
as bona fide, and the time period set in the prior notice will continue
to run.
Part IV. After-Final and Appeal Procedures
The mailing of a final Office action or the filing of a Notice of
Appeal, whichever is earlier, is a final disposition for purposes of
the 12-month goal for the pilot program. During the appeal process, the
application will be treated in accordance with the normal appeal
procedure (see MPEP chapter 1200). Any amendment, affidavit, or other
evidence submitted after a final Office action and prior to appeal must
comply with 37 CFR 1.116. The filing of an RCE for an application in
the pilot program is a final disposition for purposes of the 12-month
goal for the program. The application will not retain its special
status after the filing of a proper RCE.
Part V. Proceedings Outside the Normal Examination Process
If an application becomes involved in proceedings outside the
normal examination process (e.g., a secrecy order or petitions under 37
CFR 1.181-1.183), the USPTO will place the application in special
status under the pilot program before and after such proceedings.
During those proceedings, however, the application will not be under
special status. For example, while under a secrecy order, the
application will be treated in accordance with the normal secrecy order
procedures and will not be in special status under the pilot program.
Once the proceeding outside the normal examination process is
completed, the application will continue in special status until it
reaches a final disposition, which may occur later than 12 months from
the grant of special status under the pilot program.
Part VI. First Action Interview (FAI) Pilot Program Is Not Available
Applications accepted into the FAI Pilot Program are not eligible
for this pilot program. In addition, applications accepted into this
pilot program will not be eligible to participate in the FAI Pilot
Program. However, standard interview practices and procedures
applicable to regular ex parte prosecution will still be available. See
MPEP 713.02. For more information about the FAI Pilot Program, please
visit https://www.uspto.gov/patent/initiatives/first-action-interview/full-first-action-interview-pilot-program.
Part VII. Actions Resulting in Termination From the Pilot Program
There is no provision for withdrawal from special status under the
pilot program. However, the filing of a petition for any extension of
time under 37 CFR 1.136(a) will result in the termination of special
status under the pilot program. Presenting more than one benefit claim
to previously filed nonprovisional U.S. applications or international
applications designating the United States under 35 U.S.C. 120, 121, or
365(c) will also result in the termination of special status under the
pilot program.
An applicant may abandon the application that has been granted
special status under the pilot program in favor of a continuing
application. However, a continuing application will not automatically
be given prioritized examination status based on the request filed in
the parent application. Each application (including each continuing
application) must, on its own, meet all requirements for prioritized
examination under the pilot program.
Part VIII. Twelve-Month Goal
The objective of the pilot program is to complete, on average, the
examination of an application within 12 months of special status being
granted (i.e., within 12 months from the mailing date of the decision
granting the petition to make special). The 12-month goal is
successfully achieved when one of the following final dispositions
occurs within 12 months from the grant of special status under the
pilot program: (1) The mailing of a notice of allowance; (2) the
mailing of a final Office action; (3) the filing of an RCE; (4) the
[[Page 28935]]
abandonment of the application; or (5) the filing of a Notice of
Appeal. The final disposition of an application, however, may occur
later than the 12-month time frame in certain situations (e.g., when
the applicant filed a petition under 37 CFR 1.181). In any event,
however, the 12-month time frame is a goal. Any failure to meet the 12-
month goal, or other issues related to this goal that arise, are
neither petitionable nor appealable matters.
Applicants may shorten the overall pendency of an application in
the pilot program by replying to Office actions and notices earlier
than required by the USPTO. For example, the USPTO will endeavor to
reduce pendency, from approval of the request for prioritized
examination to final disposition, to six months if all replies occur
within 30 days of a notice by the USPTO. This goal depends on
additional factors, including the demands placed on specific examiners
by multiple co-pending applications under the pilot program. Current
statistics for prioritized examination are available at https://www.uspto.gov/corda/dashboards/patents/main.dashxml?CTNAVID=1007.
Andrei Iancu,
Under Secretary of Commerce for Intellectual Property and Director of
the United States Patent and Trademark Office.
[FR Doc. 2020-10372 Filed 5-13-20; 8:45 am]
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