Agency Information Collection Activities: Proposed Collection; Comment Request, 83499-83502 [2024-23708]
Download as PDF
Federal Register / Vol. 89, No. 200 / Wednesday, October 16, 2024 / Notices
agencies. The FSCAC will provide
advice and recommendations to the
Administrator of GSA, the FedRAMP
Board, and agencies on technical,
financial, programmatic, and
operational matters regarding the secure
adoption of cloud computing products
and services. The FSCAC will ensure
effective and ongoing coordination of
agency adoption, use, authorization,
monitoring, acquisition, and security of
cloud computing products and services
to enable agency mission and
administrative priorities. The purposes
of the Committee are:
• To examine the operations of
FedRAMP and determine ways that
authorization processes can
continuously be improved, including
the following:
Æ Measures to increase agency reuse
of FedRAMP authorizations.
Æ Proposed actions that can be
adopted to reduce the burden,
confusion, and cost associated with
FedRAMP authorizations for cloud
service providers.
Æ Measures to increase the number of
FedRAMP authorizations for cloud
computing products and services
offered by small businesses concerns (as
defined by section 3(a) of the Small
Business Act (15 U.S.C. 632(a)).
Æ Proposed actions that can be
adopted to reduce the burden and cost
of FedRAMP authorizations for
agencies.
• Collect information and feedback
on agency compliance with, and
implementation of, FedRAMP
requirements.
• Serve as a forum that facilitates
communication and collaboration
among the FedRAMP stakeholder
community.
The FSCAC will meet no fewer than
three (3) times a calendar year. Meetings
shall occur as frequently as needed,
called, and approved by the DFO.
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Purpose of the Meeting and Agenda
The November 14, 2024 public
meeting will be dedicated to continued
deliberations in order to develop an
initial draft of recommendations to the
GSA Administrator on their initial two
(2) priority initiatives of (1) identifying
and documenting top challenges and
proposing solutions around the barrier
to entry for Cloud Service Providers
(CSPs) with a focus on small businesses,
third party assessment organizations
(3PAOs), and small & large agencies,
and (2) identifying and documenting
ways to expedite the authorization
process for Cloud Service Offerings
(CSOs), such as exploring agile
authorizations and other potential cost
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reductions, both labor and financial,
with a focus on small businesses.
Members of the public will have the
opportunity to provide oral public
comments during this meeting, and may
also submit public comments in writing
prior to this meeting by completing the
public comment form on our website,
https://gsa.gov/fscac. The meeting
agenda will be posted on https://
gsa.gov/fscac prior to the meeting and
can be accessed by selecting the
‘‘Federal Secure Cloud Advisory
Committee meetings’’ tab on the left,
and then selecting the ‘‘November 14,
2024—Virtual’’ meeting accordion in
order to view all meeting materials,
agenda, and registration information.
Meeting Attendance
The virtual meeting is open to the
public. The meeting materials,
registration information, and agenda
will be made available prior to the
meeting online at https://gsa.gov/fscac,
by selecting the ‘‘Federal Secure Cloud
Advisory Committee meetings’’ tab on
the left, and then selecting the
‘‘November 14, 2024—Virtual’’ meeting
accordion. Registration for attending the
virtual meeting is highly encouraged by
5:00 p.m. EST, on Monday, November
11, 2024. After registration, individuals
will receive instructions on how to
attend the meeting via email.
For information on services for
individuals with disabilities, or to
request accommodation for a disability,
please email the FSCAC staff at
FSCAC@gsa.gov at least 10 days prior to
the meeting date. Live captioning may
be provided virtually.
Public Comment
Members of the public attending will
have the opportunity to provide oral
public comment during the FSCAC
meeting. Written public comments can
be submitted at any time by completing
the public comment form on our
website, https://gsa.gov/fscac, located
under the ‘‘Get Involved’’ section. All
written public comments will be
provided to FSCAC members in advance
of the meeting if received by
Wednesday, November 6, 2024.
Margaret Dugan
Service-Level Liaison, Federal Acquisition
Service, General Services Administration.
[FR Doc. 2024–23788 Filed 10–15–24; 8:45 am]
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83499
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
In compliance with the
Paperwork Reduction Act of 1995, this
notice announces the intention of the
Agency for Healthcare Research and
Quality (AHRQ) to request that the
Office of Management and Budget
(OMB) approve the reinstatement with
change of the information collection
project ‘‘Patient Safety Organization
Certification for Initial Listing and
Related Forms, Patient Safety
Confidentiality Complaint Form, and
Common Formats’’, OMB No. 0935–
0143 for which approval expired on
September 30, 2024. This information
collection was previously published in
the Federal Register on August 12th,
2024 and allowed 60 days for public
comment. AHRQ received no
substantive comments from members of
the public. The purpose of this notice is
to allow an additional 30 days for public
comment.
DATES: Comments on this notice must be
received by November 15, 2024.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
email REPORTSCLEARANCEOFFICER@
ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
Proposed Project
Title: Patient Safety Organization
Certification for Initial Listing and
Related Forms, Patient Safety
Confidentiality Complaint Form, and
Common Formats.
OMB No.: 0935–0143.
OMB Expiration Date: September
30th, 2024.
Type of Request: Reinstatement, with
change, of previously approved
collection for which approval has
expired.
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Federal Register / Vol. 89, No. 200 / Wednesday, October 16, 2024 / Notices
The Patient Safety and Quality
Improvement Act of 2005 (the Patient
Safety Act), signed into law on July 29,
2005, was enacted in response to
growing concern about patient safety in
the United States and the Institute of
Medicine’s 1999 report, ‘‘To Err is
Human: Building a Safer Health
System’’. The Patient Safety Act
signifies the Federal Government’s
commitment to fostering a culture of
patient safety among health care
providers; it offers a mechanism for
creating an environment in which the
causes of risks and hazards to patient
safety can be thoroughly and honestly
examined and discussed without fear of
penalties and liabilities. It provides for
the voluntary formation of Patient
Safety Organizations (PSOs) that can
collect, aggregate, and analyze
confidential information reported
voluntarily by health care providers. By
analyzing substantial amounts of patient
safety event information across multiple
institutions, PSOs are able to identify
patterns of failures and propose
measures to eliminate or reduce risks
and hazards.
In order to implement the Patient
Safety Act, the Department of Health
and Human Services (HHS) issued the
Patient Safety and Quality Improvement
Final Rule (Patient Safety Rule, 42 CFR
part 3), which became effective on
January 19, 2009. The Patient Safety
Rule outlines the requirements that
entities must meet to become and
remain listed as PSOs, the process by
which the Secretary of HHS (Secretary)
will accept certifications and list PSOs,
and provisions pertaining to the
confidentiality and privilege protections
for patient safety work product (PSWP).
When specific statutory requirements
are met, the information collected and
the analyses and deliberations regarding
the information receive confidentiality
and privilege protections under this
legislation. The Secretary delegated
authority to the Director of the Office for
Civil Rights (OCR) to interpret and
enforce the confidentiality protections
of the Patient Safety Act (Federal
Register, 71 FR 28701–2, May 17, 2006).
Civil money penalties may be imposed
for knowing or reckless impermissible
disclosures of identifiable PSWP. AHRQ
implements and administers the rest of
the statute’s provisions.
Pursuant to the Patient Safety Rule
(42 CFR 3.102), an entity that seeks to
be listed as a PSO by the Secretary must
certify that it meets certain requirements
and, upon listing, would meet other
criteria. To remain listed for renewable
three-year periods, a PSO must re-certify
that it meets these obligations and
would continue to meet them while
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listed. The Patient Safety Act and
Patient Safety Rule also impose other
obligations discussed below that a PSO
must meet to remain listed. In
accordance with the requirements of the
Patient Safety Rule (see, e.g., 42 CFR
3.102(a)(1), 3.102(b)(2)(i)(E), 3.102(d)(1),
and 3.112), the entities seeking to be
listed and to remain listed must
complete the proposed forms, in order
to attest to compliance with statutory
criteria and the corresponding
regulatory requirements.
Proposed Revisions
The following forms have revisions
for clarification which are described
below:
1. PSO Certification for Initial
Listing—This form has been revised to
include clarification on the role of the
primary point of contact.
2. PSO Certification for Continued
Listing—This form has been revised to
include clarifications on the role of the
primary point of contact, more precise
language about whether there are any
changes to the parent organization or
any additional parent organizations and
an additional note to clarify how users
should determine the response to the
standardized way they collect patient
safety work product (PSWP).
3. PSO Profile form—The form has
been revised to add a new clinical
discipline, ‘‘Clinical Dialysis Services’’.
4. PSO Change of Listing Form—This
form has been revised to note
clarifications for the parent and the
point of contact sections.
5. PSO Voluntary Relinquishment
Form—This form has been revised to
include a change from street to mailing
address for future contacts with delisted
PSOs.
6. Patient Safety Confidentiality
Complaint Form—The form has two
parts, the complaint form and the
consent form. The complaint form was
updated (1) to conform the notice to
individuals about confidentiality of
identifying information submitted on
the complaint form with the existing
approved OCR HIPAA Rules complaint
form and (2) to update OCR contact
information. The consent form was
updated (1) to conform notice to
individuals about confidentiality of
identifying information submitted on
the consent form with the existing
approved OCR HIPAA Rules consent
form, (2) to more fully describe OCR
authorities allowing collection of
information in Privacy Act of 1974
notices, and (3) to update OCR contact
information.
7. Common Formats—Since the last
approval, AHRQ has released Common
Formats Event Reporting for Diagnostic
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Safety, Version 1.0 (CFER–DS V1.0) and
the Common Formats for SurveillanceHospital V1.0 (CFS–H V1.0), which is a
revision/update from the last version
(CFS- H V0.3 Beta).
OMB previously approved the
Common Formats and forms described
above in 2008, 2011, 2014, 2018, and
2021. AHRQ will use these forms, other
than the Patient Safety Confidentiality
Complaint Form, to obtain information
necessary to carry out its authority to
implement the Patient Safety Act and
Patient Safety Rule. This includes
obtaining initial and subsequent
certifications from entities seeking to be
or remain listed as PSOs and for making
the statutorily required determinations
prior to and during an entity’s period of
listing as a PSO. The PSO Division,
housed in AHRQ’s Center for Quality
Improvement and Patient Safety, uses
this information. OCR will use the
Patient Safety Confidentiality Complaint
Form to collect information for the
initial assessment of an incoming
complaint. The form is modeled on
OCR’s form for complaints alleging
violations of the privacy of protected
health information.
Method of Collection
The PSO forms are available in a
format that allows completion and
submission of the information online.
AHRQ has updated the electronic
submission of all forms, except the
Patient Safety Confidentiality Compliant
For which is administered by OCR,
including the capability of the system to
auto populate certain fields based on
prior submissions by the PSOs. In
addition, paper forms can be
downloaded, completed and submitted
through electronic mail, to pso@
ahrq.hhs.gov, or via postal mail. The
Common Formats, accompanying user
guide, and technical specifications are
available as printable electronic files on
the PSOPPC website at
www.PSOPPC.org.
In addition to paper submission of
complaints, OCR facilitates electronic
submission of complaints. First, the
Patient Safety Confidentiality Complaint
Form is available on the OCR website at
https://www.hhs.gov/hipaa/filing-acomplaint/patient-safetyconfidentiality/. The form is
available to be downloaded
electronically to a user’s own computer
in a form that allows a complainant to
fill out the form electronically if they so
choose. The Patient Safety
Confidentiality Complaint Form can
then be printed and submitted, or
submitted electronically via electronic
mail. Second, the form is available in a
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format that allows completion and
submission of the information online.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated
annualized burden hours for the
respondent to provide the requested
information and Exhibit 2 shows the
estimated annualized cost burden
associated with the respondents’ time to
provide the requested information. The
total burden hours are estimated to be
100,811.58 hours annually and the total
cost burden is estimated to be
$4,946,824.23 annually.
1. PSO Certification for Initial Listing
Form: The average annual burden for
the collection of information requested
by the certification forms for initial
listing is based upon a total average
estimate of 11 respondents per year and
an estimated time of 18 hours per
response. The estimated response
number includes submissions by not
only entities listed as PSOs, but also
entities that submit initial listing forms
that do not become PSOs.
2. PSO Certification for Continued
Listing Form: The average annual
burden for the collection of information
requested by the certification form for
continued listing has an estimated time
of eight hours per response and 40
responses annually.
3. PSO Two Bona Fide Contracts
Requirement Certification Form: The
average annual burden for the collection
of information requested by the PSO
Two Bona Fide Contract Certification
Form is based upon an estimate of 56
respondents per year and an estimated
one hour per response.
4. PSO Disclosure Statement Form:
The overall annual burden for the
collection of information requested by
the PSO Disclosure Statement Form is
based upon an estimate of 3 respondents
per year and estimated 3 hours per
response.
5. PSO Profile Form: The overall
annual burden for the collection of
information requested by the PSO
Profile Form is based upon an estimate
of 74 respondents per year and an
estimated three hours per response.
6. PSO Change of Listing Information
Form: The average annual burden for
the collection of information requested
by the PSO Change of Listing
Information Form is based upon an
estimate of 51 respondents per year and
an estimated time of five minutes per
response.
7. PSO Voluntary Relinquishment
Form: The average annual burden for
the collection of information requested
by the PSO Voluntary Relinquishment
Form is based upon a total average
estimate of four respondents per year
and an estimated time of thirty minutes
per response.
8. OCR Patient Safety Confidentiality
Complaint Form: The overall annual
burden estimate of one hour for the
collection of information requested by
the form is based on an estimate of one
respondent per year and an estimated
twenty minutes per response.
9. Common Formats: AHRQ estimates
that 5% FTE of a patient safety manager
at a facility will be spent to administer
the Common Formats, which is
approximately 100 hours a year.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
1.
2.
3.
4.
5.
6.
7.
8.
9.
Number of
responses
per respondent
Number of
respondents
Form
Hours per
response
Total burden
Hours
PSO Certification for Initial Listing Form .........................................................
PSO Certification for Continued Listing Form .................................................
PSO Two Bona Fide Contracts Requirement Form ........................................
PSO Disclosure Statement Form ....................................................................
PSO Profile Form ............................................................................................
PSO Change of Listing Information ................................................................
PSO Voluntary Relinquishment Form .............................................................
OCR Patient Safety Confidentiality Complaint Form ......................................
Common Formats ............................................................................................
11
40
56
3
74
51
4
1
1,000
1
1
1
1
1
1
1
1
1
18
8
1
3
3
05/60
30/60
20/60
100
198
320
56
9
222
4.25
2
.33
100,000
Total ..............................................................................................................
......................
NA
NA
100,811.58
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Total
burden hours
Form
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1.
2.
3.
4.
5.
6.
7.
8.
9.
Average hourly
wage rate *
Total cost
PSO Certification for Initial Listing Form .............................................................................
PSO Certification for Continued Listing Form .....................................................................
PSO Two Bona Fide Contracts Requirement Form ...........................................................
PSO Disclosure Statement Form ........................................................................................
PSO Profile Form ................................................................................................................
PSO Change of Listing Form ..............................................................................................
PSO Voluntary Relinquishment Form .................................................................................
OCR Patient Safety Confidentiality Complaint Form ..........................................................
Common Formats ................................................................................................................
198
320
56
9
222
4.25
2
.33
100,000
$49.07
49.07
49.07
49.07
49.07
49.07
49.07
49.07
49.07
$9,715.86
15,702.40
2,747.92
441.63
10,893.54
208.55
98.14
15.35
4,907,000
Total ..................................................................................................................................
........................
............................
4,946,824.23
* Based upon the mean of the hourly average wages for healthcare practitioner and technical occupations, 29–0000, National Compensation
Survey, May 2023, ‘‘U.S. Department of Labor, Bureau of Labor Statistics.’’ https://www.bls.gov/oes/current/oes290000.htm
Request for Comments
In accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3520,
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Jkt 265001
comments on AHRQ’s information
collection are requested with regard to
any of the following: (a) whether the
proposed collection of information is
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necessary for the proper performance of
AHRQ’s health care research and health
care information dissemination
functions, including whether the
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Federal Register / Vol. 89, No. 200 / Wednesday, October 16, 2024 / Notices
information will have practical utility;
(b) the accuracy of AHRQ’s estimate of
burden (including hours and costs) of
the proposed collection(s) of
information; (c) ways to enhance the
quality, utility and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
Dated: October 3, 2024.
Marquita Cullom,
Associate Director.
[FR Doc. 2024–23708 Filed 10–15–24; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–25–0572]
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Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘CDC and
ATSDR Health Message Testing System
(HMTS)’’ to the Office of Management
and Budget (OMB) for review and
approval. CDC previously published a
‘‘Proposed Data Collection Submitted
for Public Comment and
Recommendations’’ notice on June 4,
2024 to obtain comments from the
public and affected agencies. CDC
received one non-substantive comment.
This notice serves to allow an additional
30 days for public and affected agency
comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
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including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
CDC and ATSDR Health Message
Testing System (HMTS) (OMB Control
No. 0920–0572, Exp. 10/31/2024)—
Extension—Office of Communications
(OC), Centers for Disease Control and
Prevention (CDC)
Background and Brief Description
Before CDC disseminates a health
message to the public, the message
always undergoes scientific review.
However, even though the message is
based on sound scientific content, there
is no guarantee that the public will
understand a health message or that the
message will move people to take
recommended action. Communication
theorists and researchers agree that for
health messages to be as clear and
influential as possible, target audience
members or representatives must be
involved in developing the messages
and provisional versions of the
messages must be tested with members
of the target audience. Increasingly,
there are circumstances when CDC must
move swiftly to protect life, prevent
disease, or calm public anxiety. Health
message testing is even more important
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in these instances, because of the
critical nature of the information need.
In the interest of timely health
message dissemination, many programs
forgo the important step of testing
messages on dimensions such as clarity,
salience, appeal, and persuasiveness
(i.e., the ability to influence behavioral
intention). Skipping this step avoids the
delay involved in the standard OMB
review process, but at a high potential
cost. Untested messages can waste
communication resources and
opportunities because the messages can
be perceived as unclear or irrelevant.
Untested messages can also have
unintended consequences, such as
jeopardizing the credibility of federal
health officials.
The CDC/ATSDR Health Message
Testing System (HMTS), a Generic
information collection, enables
programs across CDC and ATSDR to
collect the information they require in a
timely manner to:
• Ensure quality and prevent waste in
the dissemination of health information
by CDC to the public;
• Refine message concepts and test
draft materials for clarity, salience,
appeal, and persuasiveness to target
audiences;
• Guide the action of health
communication officials who are
responding to health emergencies,
Congressionally-mandated campaigns
with short timeframes, media-generated
public concern, time-limited
communication opportunities, trends,
and the need to refresh materials or
dissemination strategies in an ongoing
campaign.
Each testing instrument will be based
on specific health issues or topics.
Although it is not possible to develop
one instrument for use in all instances,
the same kinds of questions are asked in
most message testing. This package
includes generic questions and formats
that can be used to develop health
message testing data collection
instruments. These include a list of
screening questions, comprised of
demographic and introductory
questions, along with other questions
that can be used to create a mix of
relevant questions for each proposed
message testing data collection method.
However, programs may request to use
additional questions if needed. Message
testing questions will focus on issues
such as comprehension, impressions,
personal relevance, content and
wording, efficacy of response, channels,
and spokesperson/sponsor. Such
information will enable message
developers to enhance the effectiveness
of messages for intended audiences.
Data collection methods proposed for
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Agencies
[Federal Register Volume 89, Number 200 (Wednesday, October 16, 2024)]
[Notices]
[Pages 83499-83502]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-23708]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research and Quality, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the Paperwork Reduction Act of 1995, this
notice announces the intention of the Agency for Healthcare Research
and Quality (AHRQ) to request that the Office of Management and Budget
(OMB) approve the reinstatement with change of the information
collection project ``Patient Safety Organization Certification for
Initial Listing and Related Forms, Patient Safety Confidentiality
Complaint Form, and Common Formats'', OMB No. 0935-0143 for which
approval expired on September 30, 2024. This information collection was
previously published in the Federal Register on August 12th, 2024 and
allowed 60 days for public comment. AHRQ received no substantive
comments from members of the public. The purpose of this notice is to
allow an additional 30 days for public comment.
DATES: Comments on this notice must be received by November 15, 2024.
ADDRESSES: Written comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427-1477, or by email
[email protected].
SUPPLEMENTARY INFORMATION:
Proposed Project
Title: Patient Safety Organization Certification for Initial
Listing and Related Forms, Patient Safety Confidentiality Complaint
Form, and Common Formats.
OMB No.: 0935-0143.
OMB Expiration Date: September 30th, 2024.
Type of Request: Reinstatement, with change, of previously approved
collection for which approval has expired.
[[Page 83500]]
The Patient Safety and Quality Improvement Act of 2005 (the Patient
Safety Act), signed into law on July 29, 2005, was enacted in response
to growing concern about patient safety in the United States and the
Institute of Medicine's 1999 report, ``To Err is Human: Building a
Safer Health System''. The Patient Safety Act signifies the Federal
Government's commitment to fostering a culture of patient safety among
health care providers; it offers a mechanism for creating an
environment in which the causes of risks and hazards to patient safety
can be thoroughly and honestly examined and discussed without fear of
penalties and liabilities. It provides for the voluntary formation of
Patient Safety Organizations (PSOs) that can collect, aggregate, and
analyze confidential information reported voluntarily by health care
providers. By analyzing substantial amounts of patient safety event
information across multiple institutions, PSOs are able to identify
patterns of failures and propose measures to eliminate or reduce risks
and hazards.
In order to implement the Patient Safety Act, the Department of
Health and Human Services (HHS) issued the Patient Safety and Quality
Improvement Final Rule (Patient Safety Rule, 42 CFR part 3), which
became effective on January 19, 2009. The Patient Safety Rule outlines
the requirements that entities must meet to become and remain listed as
PSOs, the process by which the Secretary of HHS (Secretary) will accept
certifications and list PSOs, and provisions pertaining to the
confidentiality and privilege protections for patient safety work
product (PSWP).
When specific statutory requirements are met, the information
collected and the analyses and deliberations regarding the information
receive confidentiality and privilege protections under this
legislation. The Secretary delegated authority to the Director of the
Office for Civil Rights (OCR) to interpret and enforce the
confidentiality protections of the Patient Safety Act (Federal
Register, 71 FR 28701-2, May 17, 2006). Civil money penalties may be
imposed for knowing or reckless impermissible disclosures of
identifiable PSWP. AHRQ implements and administers the rest of the
statute's provisions.
Pursuant to the Patient Safety Rule (42 CFR 3.102), an entity that
seeks to be listed as a PSO by the Secretary must certify that it meets
certain requirements and, upon listing, would meet other criteria. To
remain listed for renewable three-year periods, a PSO must re-certify
that it meets these obligations and would continue to meet them while
listed. The Patient Safety Act and Patient Safety Rule also impose
other obligations discussed below that a PSO must meet to remain
listed. In accordance with the requirements of the Patient Safety Rule
(see, e.g., 42 CFR 3.102(a)(1), 3.102(b)(2)(i)(E), 3.102(d)(1), and
3.112), the entities seeking to be listed and to remain listed must
complete the proposed forms, in order to attest to compliance with
statutory criteria and the corresponding regulatory requirements.
Proposed Revisions
The following forms have revisions for clarification which are
described below:
1. PSO Certification for Initial Listing--This form has been
revised to include clarification on the role of the primary point of
contact.
2. PSO Certification for Continued Listing--This form has been
revised to include clarifications on the role of the primary point of
contact, more precise language about whether there are any changes to
the parent organization or any additional parent organizations and an
additional note to clarify how users should determine the response to
the standardized way they collect patient safety work product (PSWP).
3. PSO Profile form--The form has been revised to add a new
clinical discipline, ``Clinical Dialysis Services''.
4. PSO Change of Listing Form--This form has been revised to note
clarifications for the parent and the point of contact sections.
5. PSO Voluntary Relinquishment Form--This form has been revised to
include a change from street to mailing address for future contacts
with delisted PSOs.
6. Patient Safety Confidentiality Complaint Form--The form has two
parts, the complaint form and the consent form. The complaint form was
updated (1) to conform the notice to individuals about confidentiality
of identifying information submitted on the complaint form with the
existing approved OCR HIPAA Rules complaint form and (2) to update OCR
contact information. The consent form was updated (1) to conform notice
to individuals about confidentiality of identifying information
submitted on the consent form with the existing approved OCR HIPAA
Rules consent form, (2) to more fully describe OCR authorities allowing
collection of information in Privacy Act of 1974 notices, and (3) to
update OCR contact information.
7. Common Formats--Since the last approval, AHRQ has released
Common Formats Event Reporting for Diagnostic Safety, Version 1.0
(CFER-DS V1.0) and the Common Formats for Surveillance- Hospital V1.0
(CFS-H V1.0), which is a revision/update from the last version (CFS- H
V0.3 Beta).
OMB previously approved the Common Formats and forms described
above in 2008, 2011, 2014, 2018, and 2021. AHRQ will use these forms,
other than the Patient Safety Confidentiality Complaint Form, to obtain
information necessary to carry out its authority to implement the
Patient Safety Act and Patient Safety Rule. This includes obtaining
initial and subsequent certifications from entities seeking to be or
remain listed as PSOs and for making the statutorily required
determinations prior to and during an entity's period of listing as a
PSO. The PSO Division, housed in AHRQ's Center for Quality Improvement
and Patient Safety, uses this information. OCR will use the Patient
Safety Confidentiality Complaint Form to collect information for the
initial assessment of an incoming complaint. The form is modeled on
OCR's form for complaints alleging violations of the privacy of
protected health information.
Method of Collection
The PSO forms are available in a format that allows completion and
submission of the information online. AHRQ has updated the electronic
submission of all forms, except the Patient Safety Confidentiality
Compliant For which is administered by OCR, including the capability of
the system to auto populate certain fields based on prior submissions
by the PSOs. In addition, paper forms can be downloaded, completed and
submitted through electronic mail, to [email protected], or via postal
mail. The Common Formats, accompanying user guide, and technical
specifications are available as printable electronic files on the
PSOPPC website at www.PSOPPC.org.
In addition to paper submission of complaints, OCR facilitates
electronic submission of complaints. First, the Patient Safety
Confidentiality Complaint Form is available on the OCR website at
https://www.hhs.gov/hipaa/filing-a-complaint/patient-safety-confidentiality/. The form is available to be downloaded
electronically to a user's own computer in a form that allows a
complainant to fill out the form electronically if they so choose. The
Patient Safety Confidentiality Complaint Form can then be printed and
submitted, or submitted electronically via electronic mail. Second, the
form is available in a
[[Page 83501]]
format that allows completion and submission of the information online.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden hours for the
respondent to provide the requested information and Exhibit 2 shows the
estimated annualized cost burden associated with the respondents' time
to provide the requested information. The total burden hours are
estimated to be 100,811.58 hours annually and the total cost burden is
estimated to be $4,946,824.23 annually.
1. PSO Certification for Initial Listing Form: The average annual
burden for the collection of information requested by the certification
forms for initial listing is based upon a total average estimate of 11
respondents per year and an estimated time of 18 hours per response.
The estimated response number includes submissions by not only entities
listed as PSOs, but also entities that submit initial listing forms
that do not become PSOs.
2. PSO Certification for Continued Listing Form: The average annual
burden for the collection of information requested by the certification
form for continued listing has an estimated time of eight hours per
response and 40 responses annually.
3. PSO Two Bona Fide Contracts Requirement Certification Form: The
average annual burden for the collection of information requested by
the PSO Two Bona Fide Contract Certification Form is based upon an
estimate of 56 respondents per year and an estimated one hour per
response.
4. PSO Disclosure Statement Form: The overall annual burden for the
collection of information requested by the PSO Disclosure Statement
Form is based upon an estimate of 3 respondents per year and estimated
3 hours per response.
5. PSO Profile Form: The overall annual burden for the collection
of information requested by the PSO Profile Form is based upon an
estimate of 74 respondents per year and an estimated three hours per
response.
6. PSO Change of Listing Information Form: The average annual
burden for the collection of information requested by the PSO Change of
Listing Information Form is based upon an estimate of 51 respondents
per year and an estimated time of five minutes per response.
7. PSO Voluntary Relinquishment Form: The average annual burden for
the collection of information requested by the PSO Voluntary
Relinquishment Form is based upon a total average estimate of four
respondents per year and an estimated time of thirty minutes per
response.
8. OCR Patient Safety Confidentiality Complaint Form: The overall
annual burden estimate of one hour for the collection of information
requested by the form is based on an estimate of one respondent per
year and an estimated twenty minutes per response.
9. Common Formats: AHRQ estimates that 5% FTE of a patient safety
manager at a facility will be spent to administer the Common Formats,
which is approximately 100 hours a year.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form Number of responses per Hours per Total burden
respondents respondent response Hours
----------------------------------------------------------------------------------------------------------------
1. PSO Certification for Initial Listing Form....... 11 1 18 198
2. PSO Certification for Continued Listing Form..... 40 1 8 320
3. PSO Two Bona Fide Contracts Requirement Form..... 56 1 1 56
4. PSO Disclosure Statement Form.................... 3 1 3 9
5. PSO Profile Form................................. 74 1 3 222
6. PSO Change of Listing Information................ 51 1 05/60 4.25
7. PSO Voluntary Relinquishment Form................ 4 1 30/60 2
8. OCR Patient Safety Confidentiality Complaint Form 1 1 20/60 .33
9. Common Formats................................... 1,000 1 100 100,000
-----------------------------------------------------------
Total........................................... ............ NA NA 100,811.58
----------------------------------------------------------------------------------------------------------------
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Total burden Average hourly
Form hours wage rate \*\ Total cost
----------------------------------------------------------------------------------------------------------------
1. PSO Certification for Initial Listing Form................. 198 $49.07 $9,715.86
2. PSO Certification for Continued Listing Form............... 320 49.07 15,702.40
3. PSO Two Bona Fide Contracts Requirement Form............... 56 49.07 2,747.92
4. PSO Disclosure Statement Form.............................. 9 49.07 441.63
5. PSO Profile Form........................................... 222 49.07 10,893.54
6. PSO Change of Listing Form................................. 4.25 49.07 208.55
7. PSO Voluntary Relinquishment Form.......................... 2 49.07 98.14
8. OCR Patient Safety Confidentiality Complaint Form.......... .33 49.07 15.35
9. Common Formats............................................. 100,000 49.07 4,907,000
-------------------------------------------------
Total..................................................... .............. ................ 4,946,824.23
----------------------------------------------------------------------------------------------------------------
* Based upon the mean of the hourly average wages for healthcare practitioner and technical occupations, 29-
0000, National Compensation Survey, May 2023, ``U.S. Department of Labor, Bureau of Labor Statistics.'' https://www.bls.gov/oes/current/oes290000.htm
Request for Comments
In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501-
3520, comments on AHRQ's information collection are requested with
regard to any of the following: (a) whether the proposed collection of
information is necessary for the proper performance of AHRQ's health
care research and health care information dissemination functions,
including whether the
[[Page 83502]]
information will have practical utility; (b) the accuracy of AHRQ's
estimate of burden (including hours and costs) of the proposed
collection(s) of information; (c) ways to enhance the quality, utility
and clarity of the information to be collected; and (d) ways to
minimize the burden of the collection of information upon the
respondents, including the use of automated collection techniques or
other forms of information technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
proposed information collection. All comments will become a matter of
public record.
Dated: October 3, 2024.
Marquita Cullom,
Associate Director.
[FR Doc. 2024-23708 Filed 10-15-24; 8:45 am]
BILLING CODE 4160-90-P