Agency Information Collection Activities; Submission for OMB Review; Public Comment Request; National Center on Law and Elder Rights-Resource Support and User Satisfaction; OMB# 0985-0060, 71506-71507 [2021-27258]

Download as PDF 71506 Federal Register / Vol. 86, No. 239 / Thursday, December 16, 2021 / Notices proposing updates to Module 2 to collect additional performance data related to supplemental LIHEAP funds. Respondents: State governments, including the District of Columbia; the largest five electricity and natural gas vendors by state; the largest ten fuel oil and propane vendors by state; and state sub-grantees. ANNUAL BURDEN ESTIMATES Total number of respondents Instrument Annual number of responses per respondent Average burden hours per response Annual burden hours Module 1 (Grantee Survey) State Grantees—Module I ............................................................................... 51 1 36 1,836 51 1 200 10,200 100 1 8 800 * 1,530 1 8.5 13,005 Modules 2 and 3 (LIHEAP Performance Measures) State Grantees—Modules II and III ................................................................. Sub-Grantees (in states with sub-grantee managed systems)—Modules II and III ........................................................................................................... Energy Vendors (largest 5 electric, 5 natural gas, 10 fuel oil, and 10 propane vendors per state-average)—Modules II and III ................................. * Estimate. Estimated Total Annual Burden Hours: 25,841. Authority: 42 U.S.C. 8629(b); 42 U.S.C. 8624(b); 42 U.S.C. 8623(c). information collection within 30 days of publication of this notice to www.reginfo.gov/public/do/PRAMain. Find the information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. By mail to the Office of Information and Regulatory Affairs, OMB, New Executive Office Bldg., 725 17th St. NW, Room 10235, Washington, DC 20503, Attn: OMB Desk Officer for ACL. Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2021–27277 Filed 12–15–21; 8:45 am] BILLING CODE 4184–80–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Community Living Agency Information Collection Activities; Submission for OMB Review; Public Comment Request; National Center on Law and Elder Rights-Resource Support and User Satisfaction; OMB# 0985–0060 Administration for Community Living, HHS. ACTION: Notice. The Administration for Community Living (ACL) is announcing that the proposed collection of information listed above has been submitted to the Office of Management and Budget (OMB) for review and clearance as required under section 506(c)(2)(A) of the Paperwork Reduction Act of 1995. This 30-Day notice collects comments on the information collection requirements related to the information collection requirements for the National Center on Law and Elder RightsResource Support and User Satisfaction [OMB# 0985–0060]. DATES: Submit written comments on the collection of information by January 18, 2022. ADDRESSES: Submit written comments and recommendations for the proposed khammond on DSKJM1Z7X2PROD with NOTICES VerDate Sep<11>2014 16:54 Dec 15, 2021 Jkt 256001 Aiesha Gurley, Administration for Community Living, Washington, DC 20201, (202) 795–7358 or by email: Aiesha.Gurley@acl.hhs.gov. In compliance with 44 U.S.C. 3507, ACL has submitted the following proposed collection of information to OMB for review and clearance. ACL is requesting approval to collect data for the National Center on Law and Elder Rights-Resource Support and User Satisfaction [OMB# 0985–0060]. ACL contracts with a national legal assistance resource center, the National Center on Law and Elder Rights, to provide the required services. Through the contract, ACL provides aging, disability, and related legal professionals with training, technical assistance, complex case consultations and support for demonstration projects regarding contractually identified priority legal topics. The purpose of the information requested is for ACL to ensure that the resource center creates and prioritizes the training, case consultations and technical assistance resources it was contracted to provide and to ensure that the center targets the contractually designated aging network SUPPLEMENTARY INFORMATION: AGENCY: SUMMARY: FOR FURTHER INFORMATION CONTACT: PO 00000 Frm 00090 Fmt 4703 Sfmt 4703 practitioners about the priority subject matters. This approach enables ACL to make data-informed decisions about the deployment of its resource center assets. These data are necessary for ACL to evaluate contractual compliance with established performance indicators. These metrics include quantifiable increases in uptake by stakeholders of training, case consultation and technical assistance, and measures of satisfaction with and perceived benefit from these services. For example, the metrics measure successful problem resolution as a result of the services provided and quantifiable data on fulfillment of requests for training, technical assistance, and consultation related to the contractually designated legal and systems development topic areas. The information requested by ACL from legal and aging/disability professionals falls into the following areas: (1) Requests for training, case consultation, and technical assistance; (2) general requests for legal training (including the volume of webinar registrations), and case consultations. Comments in Response to the 60-Day Federal Register Notice A notice published in the Federal Register on, August 30, 2021 in 86 FR 48427. There were zero (0) public comments received during the response period for the 60-day notice. Estimated Program Burden: The burden hours are calculated at one (1) minute 42 seconds for each respondent to make a request for training, case consultation, or technical assistance. ACL estimates a high end of 20,000 responses with burden hours totaling 700 hours, annually. E:\FR\FM\16DEN1.SGM 16DEN1 Federal Register / Vol. 86, No. 239 / Thursday, December 16, 2021 / Notices 71507 ACL estimates the burden associated with this collection of information as follows: Number of respondents Respondent/data collection activity Annual burden hours Legal Training, Case Consultation, Technical Assistance Requests ....... Outcome Measurement ............................................................................. 20,000 5,000 1 min 42 sec .................................... 1 min 3 sec ...................................... 700 71.59 Total ................................................................................................... 25,000 4 min 39 sec .................................... 700 Dated: December 12, 2021. Alison Barkoff, Principal Deputy Administrator. [FR Doc. 2021–27258 Filed 12–15–21; 8:45 am] BILLING CODE 4154–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2021–D–0997] Referencing the Definition of ‘‘Device’’ in the Federal Food, Drug, and Cosmetic Act in Guidance, Regulatory Documents, Communications, and Other Public Documents; Draft Guidance for Industry and Food and Drug Administration Staff; Availability AGENCY: Food and Drug Administration, HHS. ACTION: Notice of availability. The Food and Drug Administration (FDA or Agency) is announcing the availability of the draft guidance entitled ‘‘Referencing the Definition of ‘Device’ in the Federal Food, Drug, and Cosmetic Act in Guidance, Regulatory Documents, Communications, and Other Public Documents.’’ FDA is issuing this draft guidance to promote clarity regarding references to the terms ‘‘device’’ and ‘‘counterfeit device’’ in guidance, regulatory documents, communications, and other public documents. This draft guidance is not final nor is it in effect at this time. DATES: Submit either electronic or written comments on the draft guidance by February 14, 2022 to ensure that the Agency considers your comment on this draft guidance before it begins work on the final version of the guidance. ADDRESSES: You may submit comments on any guidance at any time as follows: SUMMARY: khammond on DSKJM1Z7X2PROD with NOTICES Minutes per response Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. VerDate Sep<11>2014 16:54 Dec 15, 2021 Jkt 256001 Comments submitted electronically, including attachments, to https:// www.regulations.gov will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else’s Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on https://www.regulations.gov. • If you want to submit a comment with confidential information that you do not wish to be made available to the public, submit the comment as a written/paper submission and in the manner detailed (see ‘‘Written/Paper Submissions’’ and ‘‘Instructions’’). Written/Paper Submissions Submit written/paper submissions as follows: • Mail/Hand delivery/Courier (for written/paper submissions): Dockets Management Staff (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Dockets Management Staff, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in ‘‘Instructions.’’ Instructions: All submissions received must include the Docket No. FDA– 2021–D–0997 for ‘‘Referencing the Definition of ‘Device’ in the Federal Food, Drug, and Cosmetic Act in Guidance, Regulatory Documents, Communications, and Other Public Documents.’’ Received comments will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through Friday, 240–402–7500. PO 00000 Frm 00091 Fmt 4703 Sfmt 4703 • Confidential Submissions—To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ‘‘THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.’’ The Agency will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/blacked out, will be available for public viewing and posted on https://www.regulations.gov. Submit both copies to the Dockets Management Staff. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as ‘‘confidential.’’ Any information marked as ‘‘confidential’’ will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA’s posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: https:// www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to https:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852, 240–402–7500. You may submit comments on any guidance at any time (see 21 CFR 10.115(g)(5)). An electronic copy of the guidance document is available for download from the internet. See the SUPPLEMENTARY INFORMATION section for information on electronic access to the guidance. Submit written requests for a E:\FR\FM\16DEN1.SGM 16DEN1

Agencies

[Federal Register Volume 86, Number 239 (Thursday, December 16, 2021)]
[Notices]
[Pages 71506-71507]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-27258]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Community Living


Agency Information Collection Activities; Submission for OMB 
Review; Public Comment Request; National Center on Law and Elder 
Rights-Resource Support and User Satisfaction; OMB# 0985-0060

AGENCY: Administration for Community Living, HHS.

ACTION: Notice.

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

SUMMARY: The Administration for Community Living (ACL) is announcing 
that the proposed collection of information listed above has been 
submitted to the Office of Management and Budget (OMB) for review and 
clearance as required under section 506(c)(2)(A) of the Paperwork 
Reduction Act of 1995. This 30-Day notice collects comments on the 
information collection requirements related to the information 
collection requirements for the National Center on Law and Elder 
Rights-Resource Support and User Satisfaction [OMB# 0985-0060].

DATES: Submit written comments on the collection of information by 
January 18, 2022.

ADDRESSES: Submit written comments and recommendations for the proposed 
information collection within 30 days of publication of this notice to 
www.reginfo.gov/public/do/PRAMain. Find the information collection by 
selecting ``Currently under 30-day Review--Open for Public Comments'' 
or by using the search function. By mail to the Office of Information 
and Regulatory Affairs, OMB, New Executive Office Bldg., 725 17th St. 
NW, Room 10235, Washington, DC 20503, Attn: OMB Desk Officer for ACL.

FOR FURTHER INFORMATION CONTACT: Aiesha Gurley, Administration for 
Community Living, Washington, DC 20201, (202) 795-7358 or by email: 
[email protected].

SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, ACL has 
submitted the following proposed collection of information to OMB for 
review and clearance.
    ACL is requesting approval to collect data for the National Center 
on Law and Elder Rights-Resource Support and User Satisfaction [OMB# 
0985-0060]. ACL contracts with a national legal assistance resource 
center, the National Center on Law and Elder Rights, to provide the 
required services. Through the contract, ACL provides aging, 
disability, and related legal professionals with training, technical 
assistance, complex case consultations and support for demonstration 
projects regarding contractually identified priority legal topics. The 
purpose of the information requested is for ACL to ensure that the 
resource center creates and prioritizes the training, case 
consultations and technical assistance resources it was contracted to 
provide and to ensure that the center targets the contractually 
designated aging network practitioners about the priority subject 
matters.
    This approach enables ACL to make data-informed decisions about the 
deployment of its resource center assets. These data are necessary for 
ACL to evaluate contractual compliance with established performance 
indicators.
    These metrics include quantifiable increases in uptake by 
stakeholders of training, case consultation and technical assistance, 
and measures of satisfaction with and perceived benefit from these 
services. For example, the metrics measure successful problem 
resolution as a result of the services provided and quantifiable data 
on fulfillment of requests for training, technical assistance, and 
consultation related to the contractually designated legal and systems 
development topic areas. The information requested by ACL from legal 
and aging/disability professionals falls into the following areas: (1) 
Requests for training, case consultation, and technical assistance; (2) 
general requests for legal training (including the volume of webinar 
registrations), and case consultations.

Comments in Response to the 60-Day Federal Register Notice

    A notice published in the Federal Register on, August 30, 2021 in 
86 FR 48427. There were zero (0) public comments received during the 
response period for the 60-day notice.
    Estimated Program Burden: The burden hours are calculated at one 
(1) minute 42 seconds for each respondent to make a request for 
training, case consultation, or technical assistance. ACL estimates a 
high end of 20,000 responses with burden hours totaling 700 hours, 
annually.

[[Page 71507]]

    ACL estimates the burden associated with this collection of 
information as follows:

----------------------------------------------------------------------------------------------------------------
                                                   Number of                                       Annual burden
      Respondent/data collection activity         respondents         Minutes per response             hours
----------------------------------------------------------------------------------------------------------------
Legal Training, Case Consultation, Technical            20,000  1 min 42 sec....................             700
 Assistance Requests.
Outcome Measurement...........................           5,000  1 min 3 sec.....................           71.59
                                               -----------------------------------------------------------------
    Total.....................................          25,000  4 min 39 sec....................             700
----------------------------------------------------------------------------------------------------------------


    Dated: December 12, 2021.
Alison Barkoff,
Principal Deputy Administrator.
[FR Doc. 2021-27258 Filed 12-15-21; 8:45 am]
BILLING CODE 4154-01-P
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