Proposed Information Collection Activity; Adoption Call to Action Data Collection (New Data Collection), 10446-10447 [2020-03579]

Download as PDF 10446 Federal Register / Vol. 85, No. 36 / Monday, February 24, 2020 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Child Care and Development Fund (CCDF) Consumer Education Website and Reports of Serious Injuries and Death Office of Child Care, Administration for Children and Families, HHS. ACTION: Request for public comment. AGENCY: The Office of Child Care (OCC), Administration for Children and Families (ACF), U.S. Department of Health and Human Services (HHS), is proposing a revision to an approved information collection: ‘‘Child Care and Development Fund (CCDF) Consumer Education website and Reports of Serious Injuries and Death.’’ (OMB #0970–0473, expiration 2/29/2020). DATES: Comments due within 30 days of publication. OMB is required to make a SUMMARY: decision concerning the collection of information between 30 and 60 days after publication of this document in the Federal Register. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Email: OIRA_ SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration for Children and Families. Copies of the proposed collection may be obtained by emailing infocollection@ acf.hhs.gov. 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: ACF Reports Clearance Officer. All requests, ADDRESSES: emailed or written, should be identified by the title of the information collection. SUPPLEMENTARY INFORMATION: Description: The revised Consumer Education website information collection requirement will require states and territories to include certain information about their state or territory policies (related to background checks) on their Consumer Education websites. The existing Reporting of Serious Injuries and Death information collection requirement will not be modified. There are no standard federal forms associated with these reporting requirements. Respondents: The Consumer Education website information collection requirement applies to the 50 States, the District of Columbia, and five Territories that receive CCDF grants. The estimated number of provider respondents for the Reporting of Serious Injuries and Death information collection requirement would be approximately 10,000 annually. ANNUAL BURDEN ESTIMATES Instrument Annual number of respondents Consumer Education Website ....................... Reporting of Serious Injuries and Death ....... 56 States and Territories .............................. 10,000 Child Care Providers ......................... Estimated Total Annual Burden Hours: 26,800. Authority: Pub. L. 113–186; 42 U.S.C. 9858 et seq. Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2020–03557 Filed 2–21–20; 8:45 am] BILLING CODE 4184–43–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Adoption Call to Action Data Collection (New Data Collection) Administration on Children, Youth and Families, Administration for Children and Families, HHS. ACTION: Request for public comment. lotter on DSKBCFDHB2PROD with NOTICES AGENCY: The Administration on Children, Youth and Families (ACYF), Administration for Children and Families (ACF), U.S. Department of Health and Human Services (HHS), is SUMMARY: VerDate Sep<11>2014 18:30 Feb 21, 2020 Jkt 250001 Total number of responses per respondent proposing to collect data for a new descriptive study, Adoption Call to Action (ACTA) Data Collection. 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 infocollection@ acf.hhs.gov. Alternatively, copies can also be obtained by writing to the Administration for Children and Families, Office of Planning, Research and Evaluation (OPRE), 330 C Street SW, Washington, DC 20201, Attn: ACF Reports Clearance Officer. All requests, emailed or written, should be identified by the title of the information collection. SUPPLEMENTARY INFORMATION: Description: The ACTA is an effort by the ACF Children’s Bureau. The purpose of the ACTA is to engage child welfare agencies to improve the timeliness and likelihood of PO 00000 Frm 00049 Fmt 4703 Sfmt 4703 1 1 Average burden hours per response 300 1 Annual burden hours 16,800 10,000 permanency for children who are waiting for adoption. This new information collection will provide the Children’s Bureau with an understanding of agency target populations, specific strategies (interventions), and outcomes measurement, in order to inform technical assistance strategies and provide a national picture of the overall success of the initiative. Baseline data will be collected with an initial survey (Baseline Survey), followed by two administrations of a follow-up survey instrument (Progress Update Survey) designed to collect process and outcome measures at two additional points in time. The instruments focus on: (1) Identifying the target population(s) agencies are addressing, (2) understanding elements of intervention implementation (process measures), and (3) capturing information related to the outcomes of these efforts. Respondents: Respondents of these data collection instruments will include one representative from each of the 53 child welfare agencies who are participating in ACTA activities. E:\FR\FM\24FEN1.SGM 24FEN1 10447 Federal Register / Vol. 85, No. 36 / Monday, February 24, 2020 / Notices ANNUAL BURDEN ESTIMATES Total number of respondents Instrument Adoption Call to Action: Baseline Survey ............................ Adoption Call to Action: Progress Update ........................... Estimated Total Annual Burden Hours: 15. 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: Section 203 of Section II: Adoption Opportunities of the Child Abuse Prevention and Treatment Act (42 U.S.C. 5113). Molly B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2020–03579 Filed 2–21–20; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2020–N–0008] Orthopaedic and Rehabilitation Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) announces a forthcoming public advisory committee meeting of the Orthopaedic and Rehabilitation Devices Panel of the Medical Devices Advisory Committee. The general function of the committee is to provide advice and recommendations to the Agency on FDA’s regulatory issues. The meeting will be open to the public. DATES: The meeting will be held on April 23, 2020, from 8 a.m. to 6 p.m. lotter on DSKBCFDHB2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 18:30 Feb 21, 2020 Jkt 250001 Total number of responses per respondent 53 53 1 2 and on April 24, 2020, from 8 a.m. to 1 p.m. ADDRESSES: FDA White Oak Campus, 10903 New Hampshire Ave., Building 31, Conference Center, the Great Room (Rm. 1503), Silver Spring, MD 20993– 0002. Entrance for public meeting participants (non-FDA employees) is through Building 1 where routine security check procedures will be performed. For security information, please refer to https://www.fda.gov/ AboutFDA/WorkingatFDA/ BuildingsandFacilities/ WhiteOakCampusInformation/ ucm241740.htm. Answers to commonly asked questions including information regarding special accommodations due to a disability, visitor parking, and transportation may be accessed at: https://www.fda.gov/ AdvisoryCommittees/ AboutAdvisoryCommittees/ ucm408555.htm. FOR FURTHER INFORMATION CONTACT: Patricio Garcia, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 5216, Silver Spring, MD 20993–0002, Patricio.Garcia@ fda.hhs.gov, 301–796–6875, or FDA Advisory Committee Information Line, 1–800–741–8138 (301–443–0572 in the Washington, DC area). A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Therefore, you should always check the Agency’s website at https:// www.fda.gov/AdvisoryCommittees/ default.htm and scroll down to the appropriate advisory committee meeting link, or call the advisory committee information line to learn about possible modifications before coming to the meeting. SUPPLEMENTARY INFORMATION: Agenda: On April 23, 2020, during session I, the committee will discuss and make recommendations regarding the classification of facet screws systems, which are currently unclassified pre-amendment devices to class II (general and special controls). During session II, the committee will PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 Average burden hours per response .33 .25 Total burden hours Annual burden hours 18 27 6 9 discuss and make recommendations regarding the reclassification of noninvasive bone growth stimulators, which are currently post-amendment devices from class III (general controls and premarket approval) to class II (general and special controls). On April 24, 2020, the committee will discuss and make recommendations regarding the classification of three devices, which are currently unclassified pre-amendment devices to class II (general and special controls). The committee, during session I, will discuss semiconstrained toe (metatarsophalangeal) joint prostheses; during session II, will discuss intracompartmental pressure monitors; and during session III, will discuss intra-abdominal pressure monitoring devices. FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its website prior to the meeting, the background material will be made publicly available at the location of the advisory committee meeting, and the background material will be posted on FDA’s website after the meeting. Background material is available at https://www.fda.gov/ AdvisoryCommittees/ CommitteesMeetingMaterials/ default.htm. Scroll down to the appropriate advisory committee meeting link. Procedure: Interested persons may present data, information, or views, orally or in writing, on issues pending before the committee. Written submissions may be made to the contact person on or before April 1, 2020. Oral presentations from the public will be scheduled on April 23, 2020, between approximately 8:15 a.m. and 8:45 a.m. and between approximately 1 p.m. and 1:30 p.m.; on April 24, 2020, between approximately 8:15 a.m. and 9:15 a.m. Those individuals interested in making formal oral presentations should notify the contact person and indicate during which session they would like to present (see FOR FURTHER INFORMATION CONTACT). The notification should include a brief statement of the general nature of the evidence or arguments E:\FR\FM\24FEN1.SGM 24FEN1

Agencies

[Federal Register Volume 85, Number 36 (Monday, February 24, 2020)]
[Notices]
[Pages 10446-10447]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-03579]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Adoption Call to Action 
Data Collection (New Data Collection)

AGENCY: Administration on Children, Youth and Families, Administration 
for Children and Families, HHS.

ACTION: Request for public comment.

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SUMMARY: The Administration on Children, Youth and Families (ACYF), 
Administration for Children and Families (ACF), U.S. Department of 
Health and Human Services (HHS), is proposing to collect data for a new 
descriptive study, Adoption Call to Action (ACTA) Data Collection.

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 (OPRE), 330 C Street SW, Washington, 
DC 20201, Attn: ACF Reports Clearance Officer. All requests, emailed or 
written, should be identified by the title of the information 
collection.

SUPPLEMENTARY INFORMATION:
    Description: The ACTA is an effort by the ACF Children's Bureau. 
The purpose of the ACTA is to engage child welfare agencies to improve 
the timeliness and likelihood of permanency for children who are 
waiting for adoption. This new information collection will provide the 
Children's Bureau with an understanding of agency target populations, 
specific strategies (interventions), and outcomes measurement, in order 
to inform technical assistance strategies and provide a national 
picture of the overall success of the initiative. Baseline data will be 
collected with an initial survey (Baseline Survey), followed by two 
administrations of a follow-up survey instrument (Progress Update 
Survey) designed to collect process and outcome measures at two 
additional points in time. The instruments focus on: (1) Identifying 
the target population(s) agencies are addressing, (2) understanding 
elements of intervention implementation (process measures), and (3) 
capturing information related to the outcomes of these efforts.
    Respondents: Respondents of these data collection instruments will 
include one representative from each of the 53 child welfare agencies 
who are participating in ACTA activities.

[[Page 10447]]



                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                   Total number   Average burden
           Instrument              Total number    of responses      hours per     Total burden    Annual burden
                                  of respondents  per respondent     response          hours           hours
----------------------------------------------------------------------------------------------------------------
Adoption Call to Action:                      53               1             .33              18               6
 Baseline Survey................
Adoption Call to Action:                      53               2             .25              27               9
 Progress Update................
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 15.
    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: Section 203 of Section II: Adoption Opportunities of 
the Child Abuse Prevention and Treatment Act (42 U.S.C. 5113).

Molly B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2020-03579 Filed 2-21-20; 8:45 am]
BILLING CODE 4184-01-P