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