Quiero saber acerca de...

36559

Federal Register / Vol. 86, No. 130 / Monday, July 12, 2021 / Notices Administration for Community Living, Washington, DC 20201, Attention:
Susan Jenkins.
FOR FURTHER INFORMATION CONTACT:
Susan Jenkins, Administration for Community Living, Washington, DC
20201, 2027957369 or by email:
Susan.Jenkins@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the PRA 44 U.S.C. 35013520, Federal agencies must obtain approval from the Office of Management and Budget OMB for each collection of information they conduct or sponsor.
Collection of information is defined in 44 U.S.C. 35023 and 5 CFR
1320.3c and includes agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party.
The PRA requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, ACL is publishing a notice of the proposed collection of information set forth in this document.
With respect to the following collection of information, ACL invites
comments on our burden estimates or any other aspect of this collection of information, including:
1 Whether the proposed collection of information is necessary for the proper performance of ACLs functions, including whether the information will have practical utility;
2 the accuracy of ACLs estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used to determine burden estimates; 3 ways to enhance the quality, utility, and clarity of the information to be collected; and 4 ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques when appropriate, and other forms of information technology.
The Evidence Based Program Fidelity Surveys will be used by ACL to evaluate the fidelity with which ACLs grantee organizations, under the Older Americans Act, implement the required evidence-based programs. States that receive Older Americans Act funds under Title IIID are required to spend those funds on evidence-based programs to improve the health and well-being of their clients and to reduce disease and Number of respondents
Respondent/data collection activity
Estimated Program Burden ACL estimates the burden associated with this collection of information as follows:
Responses per respondent
Hours per response
Annual burden hours
Grantee: Program selection process and survey
Local Implementation Organization Survey

103
412

1
1

2.00
0.67

206
275

Total

515

1

0.93

481

Dated: July 6, 2021.
Alison Barkoff, Acting Administrator and Assistant Secretary for Aging.
FR Doc. 202114700 Filed 7921; 8:45 am BILLING CODE 415401P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration Docket No. FDA2019D1997

khammond on DSKJM1Z7X2PROD with NOTICES

injury. Since 2003, the aging services network has been steadily moving towards wider implementation of disease prevention and health promotion programs that are based on scientific evidence and demonstrated to improve the health of older adults. The FY 2012 Congressional appropriations law included, for the first time, an evidence-based requirement related to Title IIID funds.
The results of this information collection will be used by ACL/AoA to:
Effectively report its results to the President, to Congress, to the Department of Health and Human Services and to the public.
Assess the effectiveness of ACL and its grantees in monitoring program fidelity.
Aid in program refinement and continuous improvement.
To comment on this information collection please visit the ACL website:
https www.acl.gov/about-acl/publicinput.

Food and Drug Administration Oversight of Food Products Covered by Systems Recognition Arrangements; Draft Guidance for Food and Drug Administration Staff;
Availability AGENCY:

Food and Drug Administration,
HHS.
ACTION:

Notice of availability.

VerDate Sep<11>2014

17:26 Jul 09, 2021

Jkt 253001

The Food and Drug Administration FDA or Agency is announcing the availability of a draft guidance for FDA staff entitled FDA
Oversight of Food Products Covered by Systems Recognition Arrangements.
This draft guidance provides recommendations related to the FDAs regulatory oversight activities for food products imported from countries whose food safety systems the FDA has recognized in Systems Recognition Arrangements SRAs.
DATES: Submit either electronic or written comments on the draft guidance by September 10, 2021 to ensure that the Agency considers your comment on the 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:

Electronic Submissions Submit electronic comments in the following way:

PO 00000

Frm 00038

Fmt 4703

Sfmt 4703

Federal eRulemaking Portal:
https www.regulations.gov. Follow the instructions for submitting comments.
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 elses 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
E:FRFM12JYN1.SGM

12JYN1