Agency Information Collection Activities: Submission for OMB Review; Comment Request, 58919-58920 [2021-23185]

Download as PDF 58919 Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices Date: November 22, 2021. Time: 10:00 a.m. to 4:00 p.m. Eastern Time (ET). Agenda: The meeting will cover committee business items including updates on pain workforce enhancement and pain research concepts. It will include follow up of IPRCC recommendations and member updates. Webcast Live: http://videocast.nih.gov/. Deadline: Submission of intent to submit written/electronic statement for comments: Monday, November 15th, by 5:00 p.m. ET. Place: National Institutes of Health, Building 31, 31 Center Drive Bethesda, MD 20892 (Virtual Meeting). Contact Person: Linda L. Porter, Ph.D., Director, Office of Pain Policy and Planning, Office of the Director, National Institute of Neurological Disorders and Stroke, NIH, 31 Center Drive, Room 8A31, Bethesda, MD 20892, Phone: (301) 451–4460, Email: Linda.Porter@nih.gov. Any interested person may file written comments with the committee by forwarding the statement to the Contact Person listed on this notice. The statement should include the name, address, telephone number and when applicable, the business or professional affiliation of the interested person. The meeting will be open to the public via NIH Videocast https://videocast.nih.gov/. Visit the IPRCC website for more information: http://iprcc.nih.gov. Agenda and any additional information for the meeting will be posted when available. Dated: October 19, 2021. Tyeshia M. Roberson-Curtis, Program Analyst, Office of Federal Advisory Committee Policy. applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: Heart, Lung, and Blood Initial Review Group; NHLBI Institutional Training Mechanism Study Section. Date: December 10, 2021. Time: 10:00 a.m. to 6:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institute of Health, 6705 Rockledge Drive, Bethesda, MD 20817 (Virtual Meeting). Contact Person: Lindsay M. Garvin, Ph.D., Scientific Review Officer, Office of Scientific Review/DERA, National Heart, Lung, and Blood Institute, National Institutes of Health, 6705 Rockledge Drive, Room 208–Y, Bethesda, MD 20892, (301) 827–7911, lindsay.garvin@nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.233, National Center for Sleep Disorders Research; 93.837, Heart and Vascular Diseases Research; 93.838, Lung Diseases Research; 93.839, Blood Diseases and Resources Research, National Institutes of Health, HHS) Dated: October 19, 2021. David W. Freeman, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2021–23192 Filed 10–22–21; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES [FR Doc. 2021–23191 Filed 10–22–21; 8:45 am] BILLING CODE 4140–01–P Substance Abuse and Mental Health Services Administration DEPARTMENT OF HEALTH AND HUMAN SERVICES Agency Information Collection Activities: Submission for OMB Review; Comment Request National Institutes of Health Periodically, the Substance Abuse and Mental Health Services Administration (SAMHSA) will publish a summary of information collection requests under OMB review, in compliance with the Paperwork Reduction Act (44 U.S.C. chapter 35). To request a copy of these documents, call the SAMHSA Reports Clearance Officer at (240) 276–0361. jspears on DSK121TN23PROD with NOTICES1 National Heart, Lung, and Blood Institute; Notice of Closed Meeting Pursuant to section 10(d) 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 property such as patentable material, and personal information concerning individuals associated with the grant Project: Minority AIDS InitiativeManagement Reporting Tools (MAI– MRTs)—(OMB No. 0930–0357)— Revision The Substance Abuse and Mental Health Services Administration (SAMHSA), Center for Substance Abuse Prevention (CSAP) is requesting from the Office of Management and Budget (OMB) approval for the revised Minority AIDS Initiative (MAI) monitoring tools, which includes both youth and adult questionnaires as well as the quarterly progress report. This renewal includes the inclusion of new cohorts. The cohorts of grantees funded by the MAI and included in this clearance request are: • Capacity Building Initiative 2017 • Capacity Building Initiative 2018 • Prevention Navigators 2017 • Prevention Navigators 2019 • Prevention Navigators 2020 • Prevention Navigators 2021 The target population for the MAI grantees will be at-risk minority adolescents and young adults. All MAI grantees are expected to report their monitoring data using SAMHSA’s Strategic Prevention Framework (SPF) to target minority populations, as well as other high-risk groups residing in communities of color with high prevalence of Substance Abuse and HIV/AIDS. The primary objectives of the monitoring tools include: • Assess the success of the MAI in reducing risk factors and increasing protective factorsassociated with the transmission of the Human Immunodeficiency Virus (HIV), Hepatitis C Virus (HCV), and other sexually transmitted diseases (STD). • Measure the effectiveness of evidence-based programs and infrastructure development activities such as: Outreach and training, mobilization of key stakeholders, substance abuse and HIV/AIDS counseling and education, testing, referrals to appropriate medical treatment and/or other intervention strategies (i.e., cultural enrichment activities, educational and vocational resources, social marketing campaigns, and computer-based curricula). • Investigate intervention types and features that yield the best outcomes for specific population groups. • Assess the extent to which access to health care was enhanced for population groups and individuals vulnerable to behavioral health disparities residing in communities targeted by funded interventions. • Assess the process of adopting and implementing the SPF with the target populations. TABLE 1—ESTIMATES OF ANNUALIZED HOUR BURDEN Number of respondents Type of respondent activity Quarterly Progress Report ................................................. VerDate Sep<11>2014 18:00 Oct 22, 2021 Jkt 256001 PO 00000 Frm 00061 Responses per respondent 197 Fmt 4703 Sfmt 4703 Total responses 4 E:\FR\FM\25OCN1.SGM 732 25OCN1 Hours per response Total burden hours 4 2,928 58920 Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices TABLE 1—ESTIMATES OF ANNUALIZED HOUR BURDEN—Continued Number of respondents Type of respondent activity Total responses Hours per response Total burden hours Adult questionnaire ............................................................ Youth questionnaire ........................................................... 10,000 2,500 2 2 20,000 5,000 .20 .20 4,000 1000 Total ............................................................................ 12,697 .......................... 25,732 ........................ 7,928 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. Carlos Graham, Reports Clearance Officer. [FR Doc. 2021–23185 Filed 10–22–21; 8:45 am] BILLING CODE 4162–20–P DEPARTMENT OF HOMELAND SECURITY Federal Emergency Management Agency [Docket ID FEMA–2020–0016] Meetings To Implement Pandemic Response Voluntary Agreement Under Section 708 of the Defense Production Act Federal Emergency Management Agency, Department of Homeland Security. ACTION: Announcement of meetings. AGENCY: The Federal Emergency Management Agency (FEMA) is holding a series of meetings to implement the Voluntary Agreement for the Manufacture and Distribution of Critical Healthcare Resources Necessary to Respond to a Pandemic. DATES: The first meeting took place on Tuesday, October 12, 2021, from 10:00 a.m. to 12 p.m. Eastern Time (ET). The second meeting took place on Thursday, October 14, 2021, from 10:30 a.m. to 11 a.m. ET. The third meeting took place on Thursday, October 21, 2021, from 10:30 a.m. to 11 a.m. ET. The fourth meeting will take place on Thursday, October 28, 2021, from 10:30 a.m. to 11 a.m. ET. The fifth meeting will take place on Thursday, November 4, 2021, from 10:30 a.m. to 11 a.m. ET. FOR FURTHER INFORMATION CONTACT: Robert Glenn, Office of Business, Industry, Infrastructure Integration, via SUMMARY: jspears on DSK121TN23PROD with NOTICES1 Responses per respondent VerDate Sep<11>2014 18:00 Oct 22, 2021 Jkt 256001 email at OB3I@fema.dhs.gov or via phone at (202) 212–1666. SUPPLEMENTARY INFORMATION: Notice of these meetings is provided as required by section 708(h)(8) of the Defense Production Act (DPA), 50 U.S.C. 4558(h)(8), and consistent with 44 CFR part 332. The DPA authorizes the making of ‘‘voluntary agreements and plans of action’’ with representatives of industry, business, and other interests to help provide for the national defense.1 The President’s authority to facilitate voluntary agreements with respect to responding to the spread of COVID–19 within the United States was delegated to the Secretary of Homeland Security in Executive Order 13911.2 The Secretary of Homeland Security further delegated this authority to the FEMA Administrator.3 On August 17, 2020, after the appropriate consultations with the Attorney General and the Chairman of the Federal Trade Commission, FEMA completed and published in the Federal Register a ‘‘Voluntary Agreement, Manufacture and Distribution of Critical Healthcare Resources Necessary to Respond to a Pandemic’’ (Voluntary Agreement).4 Unless terminated earlier, the Voluntary Agreement is effective until August 17, 2025, and may be extended subject to additional approval by the Attorney General after consultation with the Chairman of the Federal Trade Commission. The Agreement may be used to prepare for or respond to any pandemic, including COVID–19, during that time. On December 7, 2020, the first plan of action under the Voluntary Agreement—the Plan of Action to Establish a National Strategy for the 1 50 U.S.C. 4558(c)(1). FR 18403 (Apr. 1, 2020). 3 DHS Delegation 09052, Rev. 00.1 (Apr. 1, 2020); DHS Delegation Number 09052 Rev. 00 (Jan. 3, 2017). 4 85 FR 50035 (Aug. 17, 2020). The Attorney General, in consultation with the Chairman of the Federal Trade Commission, made the required finding that the purpose of the voluntary agreement may not reasonably be achieved through an agreement having less anticompetitive effects or without any voluntary agreement and published the finding in the Federal Register on the same day. 85 FR 50049 (Aug. 17, 2020). 2 85 PO 00000 Frm 00062 Fmt 4703 Sfmt 4703 Manufacture, Allocation, and Distribution of Personal Protective Equipment (PPE) to Respond to COVID– 19 (PPE Plan of Action)—was finalized.5 The PPE Plan of Action established several sub-committees under the Voluntary Agreement, focusing on different aspects of the PPE Plan of Action. On May 24, 2021, four additional plans of action under the Voluntary Agreement—the Plan of Action to Establish a National Strategy for the Manufacture, Allocation, and Distribution of Diagnostic Test Kits and other Testing Components to respond to COVID–19, the Plan of Action to Establish a National Strategy for the Manufacture, Allocation, and Distribution of Drug Products, Drug Substances, and Associated Medical Devices to respond to COVID–19, the Plan of Action to Establish a National Strategy for the Manufacture, Allocation, and Distribution of Medical Devices to respond to COVID–19, and the Plan of Action to Establish a National Strategy for the Manufacture, Allocation, and Distribution of Medical Gases to respond to COVID–19—were finalized.6 These plans of action established several sub-committees under the Voluntary Agreement, focusing on different aspects of each plan of action. The meetings were chaired by the FEMA Administrator’s delegates from the Office of Response and Recovery (ORR) and Office of Policy and Program Analysis (OPPA), attended by the Attorney General’s delegates from the U.S. Department of Justice, and attended by the Chairman of the Federal Trade Commission’s delegates. In implementing the Voluntary Agreement, FEMA adheres to all procedural requirements of 50 U.S.C. 4558 and 44 CFR part 332. Meeting Objectives: The objectives of the meetings are as follows: 1. Meet the Sub-Committee for Oxygen under the Medical Gases Plan of Action to establish priorities related to the COVID–19 response under the Voluntary Agreement. 5 See 85 FR 78869 (Dec. 7, 2020). See also 85 FR 79020 (Dec. 8, 2020). 6 See 86 FR 27894 (May 24, 2021). See also 86 FR 28851 (May 28, 2021). E:\FR\FM\25OCN1.SGM 25OCN1

Agencies

[Federal Register Volume 86, Number 203 (Monday, October 25, 2021)]
[Notices]
[Pages 58919-58920]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-23185]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Substance Abuse and Mental Health Services Administration


Agency Information Collection Activities: Submission for OMB 
Review; Comment Request

    Periodically, the Substance Abuse and Mental Health Services 
Administration (SAMHSA) will publish a summary of information 
collection requests under OMB review, in compliance with the Paperwork 
Reduction Act (44 U.S.C. chapter 35). To request a copy of these 
documents, call the SAMHSA Reports Clearance Officer at (240) 276-0361.

Project: Minority AIDS Initiative-Management Reporting Tools (MAI-
MRTs)--(OMB No. 0930-0357)--Revision

    The Substance Abuse and Mental Health Services Administration 
(SAMHSA), Center for Substance Abuse Prevention (CSAP) is requesting 
from the Office of Management and Budget (OMB) approval for the revised 
Minority AIDS Initiative (MAI) monitoring tools, which includes both 
youth and adult questionnaires as well as the quarterly progress 
report. This renewal includes the inclusion of new cohorts.
    The cohorts of grantees funded by the MAI and included in this 
clearance request are:

 Capacity Building Initiative 2017
 Capacity Building Initiative 2018
 Prevention Navigators 2017
 Prevention Navigators 2019
 Prevention Navigators 2020
 Prevention Navigators 2021

    The target population for the MAI grantees will be at-risk minority 
adolescents and young adults. All MAI grantees are expected to report 
their monitoring data using SAMHSA's Strategic Prevention Framework 
(SPF) to target minority populations, as well as other high-risk groups 
residing in communities of color with high prevalence of Substance 
Abuse and HIV/AIDS. The primary objectives of the monitoring tools 
include:
     Assess the success of the MAI in reducing risk factors and 
increasing protective factorsassociated with the transmission of the 
Human Immunodeficiency Virus (HIV), Hepatitis C Virus (HCV), and other 
sexually transmitted diseases (STD).
     Measure the effectiveness of evidence-based programs and 
infrastructure development activities such as: Outreach and training, 
mobilization of key stakeholders, substance abuse and HIV/AIDS 
counseling and education, testing, referrals to appropriate medical 
treatment and/or other intervention strategies (i.e., cultural 
enrichment activities, educational and vocational resources, social 
marketing campaigns, and computer-based curricula).
     Investigate intervention types and features that yield the 
best outcomes for specific population groups.
     Assess the extent to which access to health care was 
enhanced for population groups and individuals vulnerable to behavioral 
health disparities residing in communities targeted by funded 
interventions.
     Assess the process of adopting and implementing the SPF 
with the target populations.

                                  Table 1--Estimates of Annualized Hour Burden
----------------------------------------------------------------------------------------------------------------
                                    Number of      Responses per       Total         Hours per      Total burden
   Type of respondent activity     respondents      respondent       responses       response          hours
----------------------------------------------------------------------------------------------------------------
Quarterly Progress Report......             197                4             732               4           2,928

[[Page 58920]]

 
Adult questionnaire............          10,000                2          20,000             .20           4,000
Youth questionnaire............           2,500                2           5,000             .20            1000
                                --------------------------------------------------------------------------------
    Total......................          12,697  ...............          25,732  ..............           7,928
----------------------------------------------------------------------------------------------------------------

    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.

Carlos Graham,
Reports Clearance Officer.
[FR Doc. 2021-23185 Filed 10-22-21; 8:45 am]
BILLING CODE 4162-20-P