Request for Public Comment: 30-Day Information Collection: Indian Health Service Forms To Implement the Privacy Rule, 64915-64917 [2023-20329]

Download as PDF 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


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