Proposed Information Collection Activity; Formative Data Collections for ACF Program Support (OMB #0970-0531), 64480-64481 [2020-22499]

Download as PDF 64480 Federal Register / Vol. 85, No. 198 / Tuesday, October 13, 2020 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [Docket No. CDC–2020–0100] Advisory Committee on Immunization Practices (ACIP); Amended Notice of Meeting Notice is hereby given of a change in the meeting of the Advisory Committee on Immunization Practices (ACIP); October 28–29, 2020, 10:00 a.m.–5:30 p.m., EDT (times subject to change), in the original Federal Register notice. The meeting, which was published in the Federal Register on September 21, 2020, Volume 85, Number 183, pages 59317–59318, is being amended and should read as follows: SUMMARY: The virtual meeting will be held on October 28–30, 2020, from 10:00 a.m.–5:30 p.m., EDT (times subject to change). The meeting is open to the public. Written comments must be received on or before October 30, 2020. ADDRESSES: For more information on ACIP please visit the ACIP website: http://www.cdc.gov/vaccines/acip/ index.html. You may submit comments, identified by Docket No. CDC–2020–0100 by any of the following methods: • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. • Mail: Docket No. CDC–2020–0100, c/o Attn: October ACIP Meeting, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H24–8, Atlanta, GA 30329–4027. Instructions: All submissions received must include the Agency name and Docket Number. All relevant comments received in conformance with the https://www.regulations.gov suitability policy will be posted without change to https://www.regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to https://www.regulations.gov. FOR FURTHER INFORMATION CONTACT: Stephanie Thomas, ACIP Committee Management Specialist, Centers for Disease Control and Prevention, khammond on DSKJM1Z7X2PROD with NOTICES DATES: National Center for Immunization and Respiratory Diseases, 1600 Clifton Road NE, MS–H24–8, Atlanta, GA 30329– 4027; Telephone: 404–639–8367; Email: ACIP@cdc.gov. SUPPLEMENTARY INFORMATION: The Director, Strategic Business Initiatives Unit, Office of the Chief Operating Officer, Centers for Disease Control and Prevention, has been delegated the authority to sign Federal Register notices pertaining to announcements of meetings and other committee management activities, for both the Centers for Disease Control and Prevention and the Agency for Toxic Substances and Disease Registry. Kalwant Smagh, Director, Strategic Business Initiatives Unit, Office of the Chief Operating Officer, Centers for Disease Control and Prevention. [FR Doc. 2020–22464 Filed 10–9–20; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Formative Data Collections for ACF Program Support (OMB #0970–0531) Office of Planning, Research, and Evaluation, Administration for Children and Families, HHS. ACTION: Request for public comment. AGENCY: The Administration for Children and Families (ACF) proposes to revise the existing overarching generic clearance for Formative Data Collections for ACF Program Support (OMB #0970–0531) to increase the estimated number of respondents and, therefore, the overall burden estimate. DATES: Comments due within 60 days of publication. In compliance with the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, ACF is soliciting public comment on the specific aspects of the information collection described above. ADDRESSES: Copies of the proposed collection of information can be obtained and comments may be forwarded by emailing OPREinfocollection@acf.hhs.gov. SUMMARY: Alternatively, copies can also be obtained by writing to the Administration for Children and Families, Office of Planning, Research and Evaluation, 330 C Street SW, Washington, DC 20201, Attn: OPRE Reports Clearance Officer. All requests emailed or written should be identified by the title of the information collection. SUPPLEMENTARY INFORMATION: Description: The goals of the generic information collections under this approval are to obtain information about program and grantee processes or needs, and to inform the following types of activities, among others: • Delivery of targeted assistance and workflows related to program and grantee processes, and the development and refinement of recordkeeping and communication systems. • Planning for provision of programmatic or evaluation-related training or technical assistance (T/TA). • Obtaining grantee or other stakeholder input on the development of program performance measures. • Use of rapid-cycle testing activities to strengthen programs in preparation for summative evaluations. ACF uses a variety of techniques such as semi-structured discussions, focus groups, surveys, templates, open-ended requests, and telephone or in-person interviews, in order to reach these goals. Following standard OMB requirements, OPRE will submit a change request for each individual data collection activity under this generic clearance. Each request will include the individual instrument(s), a justification specific to the individual information collection, and any supplementary documents. OMB should review requests within 10 days of submission. Respondents: Example respondents include: Current or prospective service providers, training or T/TA providers, grantees, contractors, current and potential participants in ACF programs or similar comparison groups, experts in fields pertaining to ACF programs, key stakeholder groups involved in ACF projects and programs, individuals engaged in program re-design or demonstration development for evaluation, state or local government officials, or others involved in or prospectively involved in ACF programs. ANNUAL BURDEN ESTIMATES Estimated total number of respondents Instrument Semi-Structured Discussions and Focus Groups ................................... VerDate Sep<11>2014 18:52 Oct 09, 2020 Jkt 253001 PO 00000 Frm 00040 Fmt 4703 Number of responses per respondent 5,000 Sfmt 4703 E:\FR\FM\13OCN1.SGM Average burden hours per response 1 13OCN1 Annual burden hours 2 10,000 64481 Federal Register / Vol. 85, No. 198 / Tuesday, October 13, 2020 / Notices ANNUAL BURDEN ESTIMATES—Continued Estimated total number of respondents Instrument Interviews ................................................................................................. Questionnaires/Surveys ........................................................................... Templates and Open-ended Requests ................................................... Estimated Total Annual Burden Hours: 20,875. Comments: The Department specifically requests comments on (a) whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to comments and suggestions submitted within 60 days of this publication. Authority: Social Security Act, Sec 1110 [42 U.S.C. 1310]. John M. Sweet Jr. ACF/OPRE Certifying Officer. [FR Doc. 2020–22499 Filed 10–9–20; 8:45 am] BILLING CODE 4184–79–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2020–N–1736] Potential Approach for Ranking of Antimicrobial Drugs According to Their Importance in Human Medicine: A Risk Management Tool for Antimicrobial New Animal Drugs; Public Meeting; Request for Comments AGENCY: Food and Drug Administration, HHS. Notice of public meeting; request for comments. ACTION: The Food and Drug Administration (FDA, the Agency, or we) is hosting a virtual public meeting entitled ‘‘Potential Approach for Ranking of Antimicrobial Drugs According to Their Importance in Human Medicine: A Risk Management Tool for Antimicrobial New Animal Drugs.’’ The purpose of the meeting is to obtain early input from the public on a potential revised approach for khammond on DSKJM1Z7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 18:52 Oct 09, 2020 Jkt 253001 Number of responses per respondent 2,500 2,500 650 considering the human medical importance of antimicrobial new animal drugs when assessing and managing the antimicrobial resistance risks associated with the use of antimicrobial drugs in animals. The Agency is seeking public input on a potential revised process for ranking antimicrobials according to their relative importance in human medicine, on the potential criteria for their ranking, and on the resulting ranked list of antimicrobial drugs. A concept paper describing this potential revised process will be made available for discussion at the public meeting and can be obtained at the website listed in section II of this notice. DATES: The public meeting will be held on November 16, 2020. Submit either electronic or written comments on this topic by January 15, 2021. Further information regarding the meeting, including the time the meeting will start, the agenda, and how to register to attend the meeting, can be found at https://www.fda.gov/animal-veterinary/ workshops-conferences-meetings/fdapublic-meeting-potential-approachranking-antimicrobial-drugs-accordingtheir-importance-human. See the SUPPLEMENTARY INFORMATION section for registration dates and information. ADDRESSES: You may submit comments as follows. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before January 15, 2021. The https://www.regulations.gov electronic filing system will accept comments until 11:59 p.m. Eastern Time at the end of January 15, 2021. Comments received by mail/hand delivery/courier (for written/paper submissions) will be considered timely if they are postmarked or the delivery service acceptance receipt is on or before that date. Electronic Submissions Submit electronic comments in the following way: • 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 PO 00000 Frm 00041 Fmt 4703 Sfmt 4703 Average burden hours per response 1 1.5 1 1 .5 10 Annual burden hours 2,500 1,875 6,500 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– 2020–N–1736 for ‘‘Potential Approach for Ranking of Antimicrobial Drugs of According to Their Importance in Human Medicine: A Risk Management Tool for Antimicrobial New Animal Drugs.’’ Received comments, those filed in a timely manner (see ADDRESSES), will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ be 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. • 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 E:\FR\FM\13OCN1.SGM 13OCN1

Agencies

[Federal Register Volume 85, Number 198 (Tuesday, October 13, 2020)]
[Notices]
[Pages 64480-64481]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-22499]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Formative Data 
Collections for ACF Program Support (OMB #0970-0531)

AGENCY: Office of Planning, Research, and Evaluation, Administration 
for Children and Families, HHS.

ACTION: Request for public comment.

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

SUMMARY: The Administration for Children and Families (ACF) proposes to 
revise the existing overarching generic clearance for Formative Data 
Collections for ACF Program Support (OMB #0970-0531) to increase the 
estimated number of respondents and, therefore, the overall burden 
estimate.

DATES: Comments due within 60 days of publication. In compliance with 
the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction 
Act of 1995, ACF is soliciting public comment on the specific aspects 
of the information collection described above.

ADDRESSES: Copies of the proposed collection of information can be 
obtained and comments may be forwarded by emailing 
[email protected]. Alternatively, copies can also be 
obtained by writing to the Administration for Children and Families, 
Office of Planning, Research and Evaluation, 330 C Street SW, 
Washington, DC 20201, Attn: OPRE Reports Clearance Officer. All 
requests emailed or written should be identified by the title of the 
information collection.

SUPPLEMENTARY INFORMATION:
    Description: The goals of the generic information collections under 
this approval are to obtain information about program and grantee 
processes or needs, and to inform the following types of activities, 
among others:
     Delivery of targeted assistance and workflows related to 
program and grantee processes, and the development and refinement of 
recordkeeping and communication systems.
     Planning for provision of programmatic or evaluation-
related training or technical assistance (T/TA).
     Obtaining grantee or other stakeholder input on the 
development of program performance measures.
     Use of rapid-cycle testing activities to strengthen 
programs in preparation for summative evaluations.
    ACF uses a variety of techniques such as semi-structured 
discussions, focus groups, surveys, templates, open-ended requests, and 
telephone or in-person interviews, in order to reach these goals.
    Following standard OMB requirements, OPRE will submit a change 
request for each individual data collection activity under this generic 
clearance. Each request will include the individual instrument(s), a 
justification specific to the individual information collection, and 
any supplementary documents. OMB should review requests within 10 days 
of submission.
    Respondents: Example respondents include: Current or prospective 
service providers, training or T/TA providers, grantees, contractors, 
current and potential participants in ACF programs or similar 
comparison groups, experts in fields pertaining to ACF programs, key 
stakeholder groups involved in ACF projects and programs, individuals 
engaged in program re-design or demonstration development for 
evaluation, state or local government officials, or others involved in 
or prospectively involved in ACF programs.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                 Estimated        Number of     Average  burden
                 Instrument                   total number of   responses per      hours  per     Annual  burden
                                                respondents       respondent        response          hours
----------------------------------------------------------------------------------------------------------------
Semi-Structured Discussions and Focus Groups            5,000                1                2           10,000

[[Page 64481]]

 
Interviews..................................            2,500                1                1            2,500
Questionnaires/Surveys......................            2,500              1.5               .5            1,875
Templates and Open-ended Requests...........              650                1               10            6,500
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 20,875.
    Comments: The Department specifically requests comments on (a) 
whether the proposed collection of information is necessary for the 
proper performance of the functions of the agency, including whether 
the information shall have practical utility; (b) the accuracy of the 
agency's estimate of the burden of the proposed collection of 
information; (c) the quality, utility, and clarity of the information 
to be collected; and (d) ways to minimize the burden of the collection 
of information on respondents, including through the use of automated 
collection techniques or other forms of information technology. 
Consideration will be given to comments and suggestions submitted 
within 60 days of this publication.

    Authority: Social Security Act, Sec 1110 [42 U.S.C. 1310].

John M. Sweet Jr.
ACF/OPRE Certifying Officer.
[FR Doc. 2020-22499 Filed 10-9-20; 8:45 am]
BILLING CODE 4184-79-P