Request for Public Comment: 30-Day Information Collection: Indian Health Service Forms To Implement the Privacy Rule, 64915-64917 [2023-20329]
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Federal Register / Vol. 88, No. 181 / Wednesday, September 20, 2023 / Notices
following subjects: (1) The necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions; (2) the accuracy
of the estimated burden; (3) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(4) the use of automated collection
techniques or other forms of information
technology to minimize the information
collection burden.
64915
requirement of all TPP awards and is
included in the NOFOs. The data
collection will allow OPA to comply
with federal accountability and
performance requirements, inform
stakeholders of grantee progress in
meeting TPP program goals, provide
OPA with metrics for monitoring TPP
grantees, and facilitate individual
grantees’ continuous quality
improvement efforts within their
projects. OPA requests clearance for one
year to cover reporting during the nocost extension period of the awards.
Title of the Collection
Type of Collection: Reinstatement
without change.
OMB No.: 0990–0438.
Abstract: The Office of Population
Affairs (OPA), in the Office of the
Assistant Secretary for Health (OASH),
U.S. Department of Health and Human
Services (HHS), requests clearance for
the collection of performance measures
specifically for FY2020 Teen Pregnancy
Prevention (TPP) Program grantees.
Collection of performance measures is a
ESTIMATED ANNUALIZED BURDEN TABLE
Partners and sustainability ...............
Training .............................................
Dissemination ...................................
Stakeholder Engagement .................
Reach and Demographics ................
Dosage ..............................................
Fidelity and Quality ...........................
Tier 2 Innovation Network ................
Supportive Services (Tier 1) .............
All TPP grantees ..............................
All TPP Grantees .............................
All TPP Grantees .............................
All TPP Grantees .............................
Tier 1 and Tier 2 Phase II Grantees
Tier 1 and Tier 2 Phase II Grantees
Tier 1 and Tier 2 Phase II Grantees
Tier 2 Innovation Network Grantees
Tier 1 Grantees ................................
90
90
90
90
64
64
64
14
54
2
2
2
2
2
2
2
2
2
15/60
15/60
30/60
15/60
3
2
2
15/60
15/60
45
45
90
45
384
256
256
7
27
Total ...........................................
...........................................................
........................
2
........................
1155
[FR Doc. 2023–20290 Filed 9–19–23; 8:45 am]
BILLING CODE 4150–34–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Indian Health Service
Request for Public Comment: 30-Day
Information Collection: Indian Health
Service Forms To Implement the
Privacy Rule
AGENCY:
Indian Health Service, HHS.
Notice and request for
comments; request for extension of
approval.
ACTION:
In compliance with the
Paperwork Reduction Act of 1995, the
Indian Health Service (IHS) invites the
general public to comment on the
information collection titled, ‘‘IHS
Forms to Implement the Privacy Rule’’
Office of Management and Budget
(OMB) Control Number 0917–0030. This
notice announces the IHS intent to
submit the collection, which expires
September 30, 2023, to OMB for
approval of an extension with
modifications, and to solicit comments
SUMMARY:
lotter on DSK11XQN23PROD with NOTICES1
Average
burden per
response
(in hours)
Type of
respondent
Sherrette A. Funn,
Paperwork Reduction Act Reports Clearance
Officer, Office of the Secretary.
VerDate Sep<11>2014
16:38 Sep 19, 2023
Jkt 259001
Number of
respondents
Number
responses per
respondent
Form
on specific aspects of the information
collection.
Comment Due Date: October 20,
2023. Your comments regarding this
information collection are best assured
of having full effect if received within
30 days of the date of this publication.
ADDRESSES: Send your comments and
suggestions regarding the proposed
information collection contained in this
notice, especially regarding the
estimated public burden and associated
response time to: Office of Management
and Budget, Office of Regulatory Affairs,
New Executive Office Building, Room
10235, Washington, DC 20503,
Attention: Desk Officer for IHS.
FOR FURTHER INFORMATION CONTACT: To
request additional information, please
contact Evonne Bennett, Information
Collection Clearance Officer, by email:
Evonne.Bennett@ihs.gov or (240) 472–
1996.
DATES:
The IHS
published a notice on this previously
approved information collection in the
Federal Register (88 FR 42726) on July
3, 2023, and allowed 60 days for public
comment. No public comment was
received in response to the notice. The
purpose of this notice is to allow 30
days for public comment to be
submitted to OMB. A copy of the
supporting statement is available at
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
Total burden
hours
www.regulations.gov (see Docket ID
IHS_FRDOC_0001).
Title of Collection: 0917–0030, IHS
Forms to Implement the Privacy Rule
(45 CFR parts 160 & 164). Type of
Information Collection Request:
Extension of the currently approved
information collection, with
modifications 0917–0030, IHS Forms to
Implement the Privacy Rule (45 CFR
parts 160 & 164). Form(s): IHS–810,
IHS–912–1, IHS–912–2, IHS–913, IHS–
917, IHS–982, and IHS–963. Need and
Use of Information Collection: This
collection of information is made
necessary by the Department of Health
and Human Services Rule entitled
‘‘Standards for Privacy of Individually
Identifiable Health Information’’
(Privacy Rule) (45 CFR parts 160 and
164). The Privacy Rule implements the
privacy requirements of the
Administrative Simplification subtitle
of the Health Insurance Portability and
Accountability Act of 1996, creates
national standards to protect an
individual’s personal health
information, and gives patients
increased access to their medical
records. 45 CFR 164.508, 164.520,
164.522, 164.526 and 164.528 of the
Rule require the collection of
information to implement these
protection standards and access
requirements. The IHS will use the
E:\FR\FM\20SEN1.SGM
20SEN1
64916
Federal Register / Vol. 88, No. 181 / Wednesday, September 20, 2023 / Notices
following data collection instruments to
meet the information collection
requirements contained in the Rule.
(a) 45 CFR 164.508—Authorization for
Use or Disclosure of Protected Health
Information (IHS–810)
45 CFR 164.508 requires covered
entities to obtain or receive a valid
authorization for its use or disclosure of
protected health information for
purposes that are not otherwise
authorized or required by HIPAA (e.g.,
treatment, payment and healthcare
operations). Under this provision,
individuals may initiate a written
authorization permitting covered
entities to release their protected health
information to entities of their choosing.
The form IHS–810 ‘‘Authorization for
Use or Disclosure of Protected Health
Information’’ is used by patients at IHS
facilities to document and authorize the
use, disclosure or release of their
protected health information from their
medical record to anyone they specify.
(b) 45 CFR 164.522(a)(1)—Request For
Restriction(s) (IHS–912–1)
Under the Privacy Rule, an individual
can request to restrict the use of their
information with some exceptions.
Section 164.522(a)(1) requires a covered
entity to permit individuals to request
that the covered entity restrict certain
uses and disclosures of their protected
health information. The covered entity
may or may not agree to the restriction,
and it is only required to agree in
certain limited situations. The form
IHS–912–1 ‘‘Request for Restrictions(s)’’
is used to document an individual’s
request for restriction of their protected
health information and whether IHS
agreed or disagreed with the requested
restriction.
(c) 45 CFR 164.522(a)(2)—Request For
Revocation of Restriction(s) (IHS–912–
2)
Section 164.522(a)(2) permits a
covered entity to terminate its
agreement to a restriction when the
individual agrees to or requests the
termination in writing. The form IHS–
912–2 ‘‘Request for Revocation of
Restriction(s)’’ is used to document the
agency or individual request to
terminate a formerly agreed to
restriction regarding the use and
disclosure of protected health
information. A previous request to
restrict information may be revoked by
the individual or IHS, subject to the
limitations set forth in 164.522(a)(2).
(d) 45 CFR 164.528 and HHS Privacy
Act Regulations, 45 CFR 5b.9(c)—
Request for an Accounting of
Disclosures (IHS–913)
These provisions require the IHS, as
a covered entity and an agency within
HHS, to permit individuals to request
that the IHS provide an accounting of
disclosures of the individual’s protected
health information and/or record. The
form IHS–913 ‘‘Request for an
Accounting of Disclosures’’ is used for
the collection of information for the
purpose of processing an accounting of
disclosures requested by the patient
and/or personal representative, and to
document that request.
(e) 45 CFR 164.526—Request for
Correction/Amendment of Protected
Health Information (IHS–917)
This provision requires covered
entities to permit an individual to
request that the covered entity amend
protected health information. If the
covered entity accepts the requested
amendment, in whole or in part, the
covered entity must inform the
individual that the request for an
amendment is accepted. If the covered
entity denies the requested amendment,
in whole or in part, the covered entity
must provide the individual with a
written denial. The IHS developed the
form (IHS–917) to permit individuals to
submit their request and to document
IHS’s acceptance or denial of a patient’s
request to correct or amend their
protected health information.
(f) 45 CFR 164.520—Acknowledgement
of Receipt of the IHS Notice of Privacy
Practices (IHS–982)
This provision requires covered
entities to provide a Notice of Privacy
Practices to patients and to document
compliance with the notice
requirements by retaining copies of
written acknowledgments of the receipt
of the notice or documentation of good
faith efforts to obtain written
acknowledgment. The IHS developed
the form (IHS–982) to obtain the written
acknowledgment of the receipt of the
IHS Notice of Privacy Practices.
(g) 45 CFR 164.522—Request for
Confidential Communication by
Alternative Means or Alternate
Location (IHS–963)
This provision requires covered
entities to permit individuals to request
and must accommodate reasonable
requests by individuals to receive
communications of protected health
information from the covered health
care provider by alternative means or at
alterative locations. The IHS developed
the form (IHS–963) to permit
individuals to request communications
by alternative means or locations.
Completed forms used in this
collection of information are filed in the
IHS ‘‘Medical, Health and Billing
Records,’’ a Privacy Act System of
Records. Affected Public: Individuals
and households. Type of Respondents:
Individuals. Burden Hours: The table
below provides the following details for
this information collection: types of data
collection instruments, estimated
number of respondents, number of
responses per respondent, average
burden hour per response.
TABLE—ESTIMATED ANNUAL BURDEN HOURS
Estimated
number of
respondents
lotter on DSK11XQN23PROD with NOTICES1
Data collection instruments
‘‘Authorization for Use or Disclosure of Protected Health Information’’ (OMB
No. 0917–0030, IHS–810) ...........................................................................
‘‘Request for Restriction(s)’’ (OMB No. 0917–0030, IHS–912–1) ...................
‘‘Request for Revocation of Restriction(s)’’ (OMB No. 0917–0030, IHS–912–
2) ..................................................................................................................
‘‘Request for Accounting of Disclosures’’ (OMB No. 0917–0030, IHS–913) ..
‘‘Request for Correction/Amendment of Protected Health Information’’ (OMB
No. 0917–0030, IHS–917) ...........................................................................
Acknowledgement of Receipt of the Notice of Privacy Practices Protected
Health Information (IHS–982) ......................................................................
VerDate Sep<11>2014
16:38 Sep 19, 2023
Jkt 259001
PO 00000
Frm 00036
Fmt 4703
Sfmt 4703
Responses
per
respondent
Average
burden hour
per response *
Total annual
burden hours
210,954
214
1
1
10/60
10/60
35,159
36
3
39
1
1
10/60
10/60
.5
6.5
54
1
10/60
9
39
1
10/60
6.5
E:\FR\FM\20SEN1.SGM
20SEN1
Federal Register / Vol. 88, No. 181 / Wednesday, September 20, 2023 / Notices
64917
TABLE—ESTIMATED ANNUAL BURDEN HOURS—Continued
Estimated
number of
respondents
Data collection instruments
Responses
per
respondent
Average
burden hour
per response *
Total annual
burden hours
‘‘Request for Confidential Communication by Alternative Means or Alternate
Location’’ No. 0917–0030 (IHS–963) ...........................................................
214
1
10/60
36
Total Annual Burden .................................................................................
211,303
........................
........................
35,253.5
* For ease of understanding, burden hours are provided in actual minutes.
The total estimated burden for this
collection of information is 35,253.5
hours.
There are no capital costs, operating
costs and/or maintenance costs to
respondents to report.
Requests for Comments: Your written
comments and/or suggestions are
invited on one or more of the following
points:
(a) Whether the information collection
activity is necessary to carry out an
agency function;
(b) Whether the agency processes the
information collected in a useful and
timely fashion;
(c) The accuracy of the public burden
estimate (the estimated amount of time
needed for individual respondents to
provide the requested information);
(d) Whether the methodology and
assumptions used to determine the
estimates are logical;
(e) Ways to enhance the quality,
utility, and clarity of the information
being collected; and
(f) ways to minimize the public
burden through the use of automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology.
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: National Institute of
Allergy and Infectious Diseases Special
Emphasis Panel; NIAID Investigator Initiated
Program Project Applications (P01 Clinical
Trial Not Allowed).
Date: October 24, 2023.
Time: 10:00 a.m. to 2:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute of Allergy and
Infectious Diseases, National Institutes of
Health, 5601 Fishers Lane, Room 3G13,
Rockville, MD 20892 (Virtual Meeting).
Contact Person: Mairi Noverr, Ph.D.,
Scientific Review Officer, Scientific Review
Program, Division of Extramural Activities,
National Institute of Allergy and Infectious
Diseases, National Institutes of Health, 5601
Fishers Lane, Room 3G13, Rockville, MD
20852, (240) 747–7530, mairi.noverr@
nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.855, Allergy, Immunology,
and Transplantation Research; 93.856,
Microbiology and Infectious Diseases
Research, National Institutes of Health, HHS)
[FR Doc. 2023–20329 Filed 9–19–23; 8:45 am]
Dated: September 14, 2023.
Tyeshia M. Roberson-Curtis,
Program Analyst, Office of Federal Advisory
Committee Policy.
BILLING CODE 4165–16–P
[FR Doc. 2023–20326 Filed 9–19–23; 8:45 am]
Roselyn Tso,
Director, Health Service.
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
lotter on DSK11XQN23PROD with NOTICES1
National Institute of Allergy and
Infectious Diseases; Notice of Closed
Meeting
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting 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
VerDate Sep<11>2014
16:38 Sep 19, 2023
Jkt 259001
National Institutes of Health
National Institute of Neurological
Disorders and Stroke; Notice of Closed
Meetings
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, 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
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
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: National Institute of
Neurological Disorders and Stroke Initial
Review Group; Neurological Sciences and
Disorders C Study Section Translational
Neural, Brain, and Pain Relief Devices (NSD–
C).
Date: October 17–18, 2023.
Time: 9:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Canopy by Hilton, 940 Rose Avenue,
North Bethesda, MD 20852.
Contact Person: Ana Olariu, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, Division of Extramural Activities,
NINDS/NIH, NSC, 6001 Executive Blvd.,
Rockville, MD 20852, 301–496–9223,
ana.olariu@nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Initial
Review Group; Neurological Sciences and
Disorders B Study Section.
Date: October 19–20, 2023.
Time: 10:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Intercontinental San Francisco, 888
Howard Street, San Francisco, CA 94103.
Contact Person: Joel A. Saydoff, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, Division of Extramural Activities,
NINDS/NIH, NSC, 6001 Executive Blvd.,
Rockville, MD 20852, 301–496–9223,
joel.saydoff@nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Special
Emphasis Panel; BRAIN Initiative: Research
Resource Grants for Technology Integration
and Dissemination (U24 Clinical Trial Not
Allowed).
Date: October 26, 2023.
Time: 10:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852 (Virtual
Meeting).
Contact Person: Bo-Shiun Chen, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, Division of Extramural Activities,
NINDS/NIH, NSC, 6001 Executive Blvd.,
Rockville, MD 20852, 301–496–9223, boshiun.chen@nih.gov.
E:\FR\FM\20SEN1.SGM
20SEN1
Agencies
[Federal Register Volume 88, Number 181 (Wednesday, September 20, 2023)]
[Notices]
[Pages 64915-64917]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-20329]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Indian Health Service
Request for Public Comment: 30-Day Information Collection: Indian
Health Service Forms To Implement the Privacy Rule
AGENCY: Indian Health Service, HHS.
ACTION: Notice and request for comments; request for extension of
approval.
-----------------------------------------------------------------------
SUMMARY: In compliance with the Paperwork Reduction Act of 1995, the
Indian Health Service (IHS) invites the general public to comment on
the information collection titled, ``IHS Forms to Implement the Privacy
Rule'' Office of Management and Budget (OMB) Control Number 0917-0030.
This notice announces the IHS intent to submit the collection, which
expires September 30, 2023, to OMB for approval of an extension with
modifications, and to solicit comments on specific aspects of the
information collection.
DATES: Comment Due Date: October 20, 2023. Your comments regarding this
information collection are best assured of having full effect if
received within 30 days of the date of this publication.
ADDRESSES: Send your comments and suggestions regarding the proposed
information collection contained in this notice, especially regarding
the estimated public burden and associated response time to: Office of
Management and Budget, Office of Regulatory Affairs, New Executive
Office Building, Room 10235, Washington, DC 20503, Attention: Desk
Officer for IHS.
FOR FURTHER INFORMATION CONTACT: To request additional information,
please contact Evonne Bennett, Information Collection Clearance
Officer, by email: [email protected] or (240) 472-1996.
SUPPLEMENTARY INFORMATION: The IHS published a notice on this
previously approved information collection in the Federal Register (88
FR 42726) on July 3, 2023, and allowed 60 days for public comment. No
public comment was received in response to the notice. The purpose of
this notice is to allow 30 days for public comment to be submitted to
OMB. A copy of the supporting statement is available at
www.regulations.gov (see Docket ID IHS_FRDOC_0001).
Title of Collection: 0917-0030, IHS Forms to Implement the Privacy
Rule (45 CFR parts 160 & 164). Type of Information Collection Request:
Extension of the currently approved information collection, with
modifications 0917-0030, IHS Forms to Implement the Privacy Rule (45
CFR parts 160 & 164). Form(s): IHS-810, IHS-912-1, IHS-912-2, IHS-913,
IHS-917, IHS-982, and IHS-963. Need and Use of Information Collection:
This collection of information is made necessary by the Department of
Health and Human Services Rule entitled ``Standards for Privacy of
Individually Identifiable Health Information'' (Privacy Rule) (45 CFR
parts 160 and 164). The Privacy Rule implements the privacy
requirements of the Administrative Simplification subtitle of the
Health Insurance Portability and Accountability Act of 1996, creates
national standards to protect an individual's personal health
information, and gives patients increased access to their medical
records. 45 CFR 164.508, 164.520, 164.522, 164.526 and 164.528 of the
Rule require the collection of information to implement these
protection standards and access requirements. The IHS will use the
[[Page 64916]]
following data collection instruments to meet the information
collection requirements contained in the Rule.
(a) 45 CFR 164.508--Authorization for Use or Disclosure of Protected
Health Information (IHS-810)
45 CFR 164.508 requires covered entities to obtain or receive a
valid authorization for its use or disclosure of protected health
information for purposes that are not otherwise authorized or required
by HIPAA (e.g., treatment, payment and healthcare operations). Under
this provision, individuals may initiate a written authorization
permitting covered entities to release their protected health
information to entities of their choosing. The form IHS-810
``Authorization for Use or Disclosure of Protected Health Information''
is used by patients at IHS facilities to document and authorize the
use, disclosure or release of their protected health information from
their medical record to anyone they specify.
(b) 45 CFR 164.522(a)(1)--Request For Restriction(s) (IHS-912-1)
Under the Privacy Rule, an individual can request to restrict the
use of their information with some exceptions. Section 164.522(a)(1)
requires a covered entity to permit individuals to request that the
covered entity restrict certain uses and disclosures of their protected
health information. The covered entity may or may not agree to the
restriction, and it is only required to agree in certain limited
situations. The form IHS-912-1 ``Request for Restrictions(s)'' is used
to document an individual's request for restriction of their protected
health information and whether IHS agreed or disagreed with the
requested restriction.
(c) 45 CFR 164.522(a)(2)--Request For Revocation of Restriction(s)
(IHS-912-2)
Section 164.522(a)(2) permits a covered entity to terminate its
agreement to a restriction when the individual agrees to or requests
the termination in writing. The form IHS-912-2 ``Request for Revocation
of Restriction(s)'' is used to document the agency or individual
request to terminate a formerly agreed to restriction regarding the use
and disclosure of protected health information. A previous request to
restrict information may be revoked by the individual or IHS, subject
to the limitations set forth in 164.522(a)(2).
(d) 45 CFR 164.528 and HHS Privacy Act Regulations, 45 CFR 5b.9(c)--
Request for an Accounting of Disclosures (IHS-913)
These provisions require the IHS, as a covered entity and an agency
within HHS, to permit individuals to request that the IHS provide an
accounting of disclosures of the individual's protected health
information and/or record. The form IHS-913 ``Request for an Accounting
of Disclosures'' is used for the collection of information for the
purpose of processing an accounting of disclosures requested by the
patient and/or personal representative, and to document that request.
(e) 45 CFR 164.526--Request for Correction/Amendment of Protected
Health Information (IHS-917)
This provision requires covered entities to permit an individual to
request that the covered entity amend protected health information. If
the covered entity accepts the requested amendment, in whole or in
part, the covered entity must inform the individual that the request
for an amendment is accepted. If the covered entity denies the
requested amendment, in whole or in part, the covered entity must
provide the individual with a written denial. The IHS developed the
form (IHS-917) to permit individuals to submit their request and to
document IHS's acceptance or denial of a patient's request to correct
or amend their protected health information.
(f) 45 CFR 164.520--Acknowledgement of Receipt of the IHS Notice of
Privacy Practices (IHS-982)
This provision requires covered entities to provide a Notice of
Privacy Practices to patients and to document compliance with the
notice requirements by retaining copies of written acknowledgments of
the receipt of the notice or documentation of good faith efforts to
obtain written acknowledgment. The IHS developed the form (IHS-982) to
obtain the written acknowledgment of the receipt of the IHS Notice of
Privacy Practices.
(g) 45 CFR 164.522--Request for Confidential Communication by
Alternative Means or Alternate Location (IHS-963)
This provision requires covered entities to permit individuals to
request and must accommodate reasonable requests by individuals to
receive communications of protected health information from the covered
health care provider by alternative means or at alterative locations.
The IHS developed the form (IHS-963) to permit individuals to request
communications by alternative means or locations.
Completed forms used in this collection of information are filed in
the IHS ``Medical, Health and Billing Records,'' a Privacy Act System
of Records. Affected Public: Individuals and households. Type of
Respondents: Individuals. Burden Hours: The table below provides the
following details for this information collection: types of data
collection instruments, estimated number of respondents, number of
responses per respondent, average burden hour per response.
Table--Estimated Annual Burden Hours
----------------------------------------------------------------------------------------------------------------
Estimated Average burden
Data collection instruments number of Responses per hour per Total annual
respondents respondent response * burden hours
----------------------------------------------------------------------------------------------------------------
``Authorization for Use or Disclosure of 210,954 1 10/60 35,159
Protected Health Information'' (OMB No. 0917-
0030, IHS-810).................................
``Request for Restriction(s)'' (OMB No. 0917- 214 1 10/60 36
0030, IHS-912-1)...............................
``Request for Revocation of Restriction(s)'' 3 1 10/60 .5
(OMB No. 0917-0030, IHS-912-2).................
``Request for Accounting of Disclosures'' (OMB 39 1 10/60 6.5
No. 0917-0030, IHS-913)........................
``Request for Correction/Amendment of Protected 54 1 10/60 9
Health Information'' (OMB No. 0917-0030, IHS-
917)...........................................
Acknowledgement of Receipt of the Notice of 39 1 10/60 6.5
Privacy Practices Protected Health Information
(IHS-982)......................................
[[Page 64917]]
``Request for Confidential Communication by 214 1 10/60 36
Alternative Means or Alternate Location'' No.
0917-0030 (IHS-963)............................
---------------------------------------------------------------
Total Annual Burden........................ 211,303 .............. .............. 35,253.5
----------------------------------------------------------------------------------------------------------------
* For ease of understanding, burden hours are provided in actual minutes.
The total estimated burden for this collection of information is
35,253.5 hours.
There are no capital costs, operating costs and/or maintenance
costs to respondents to report.
Requests for Comments: Your written comments and/or suggestions are
invited on one or more of the following points:
(a) Whether the information collection activity is necessary to
carry out an agency function;
(b) Whether the agency processes the information collected in a
useful and timely fashion;
(c) The accuracy of the public burden estimate (the estimated
amount of time needed for individual respondents to provide the
requested information);
(d) Whether the methodology and assumptions used to determine the
estimates are logical;
(e) Ways to enhance the quality, utility, and clarity of the
information being collected; and
(f) ways to minimize the public burden through the use of
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology.
Roselyn Tso,
Director, Health Service.
[FR Doc. 2023-20329 Filed 9-19-23; 8:45 am]
BILLING CODE 4165-16-P