Proposed Information Collection Activity; Comment Request, 23684-23685 [2018-10910]
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23684
Federal Register / Vol. 83, No. 99 / Tuesday, May 22, 2018 / Notices
ANNUAL BURDEN ESTIMATES
Information collection instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Registration Screens .......................................................................................
648
1
0.15
97.20
Estimated Total Annual Burden
Hours: 97.20.
In compliance with the requirements
of the Paperwork Reduction Act of 1995
(Pub. L. 104–13, 44 U.S.C. Chap 35), the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded 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. Email
address: infocollection@acf.hhs.gov. All
requests should be identified by the title
of the information collection.
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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2018–10888 Filed 5–21–18; 8:45 am]
BILLING CODE 4184–41–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
[OMB No.: 0970–0204]
Submission for OMB Review;
Comment Request; Grants to States
for Access and Visitation
Description: On an annual basis,
States must provide OCSE with data on
programs that the Grants to States for
Access and Visitation Program has
funded. These program reporting
requirements include, but are not
limited to, the collection of data on the
number of parents served, types of
services delivered, program outcomes,
client socio economic data, referrals
sources, and other relevant data.
Respondents: State Child Access and
Visitation Programs and State and/or
Local Service Providers.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instruments: state and local child access program survey
amozie on DSK3GDR082PROD with NOTICES1
Part I: 54 states/jurisdictions ...........................................................................
Part II: 296 local service grantees (estimated) ................................................
Estimated Total Annual Burden
Hours: 5600.
Additional Information:
Copies of the proposed collection may
be obtained by writing to the
Administration for Children and
Families, Office of Planning Research
and Evaluation, 330 C Street SW,
Washington, DC, 20201. Attention
Reports Clearance Officer. All requests
should be identified by title of the
information collection. Email address:
infocollection@acf.hhs.gov.
OMB Comment:
OMB is required to make a 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
VerDate Sep<11>2014
16:47 May 21, 2018
Jkt 241001
54
296
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
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2018–10820 Filed 5–21–18; 8:45 am]
BILLING CODE 4184–41–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects:
Title: Federal Child Support Portal
Registration.
PO 00000
Frm 00060
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
1
1
Average
burden hours
per response
16
16
Total burden
hours
864
4736
OMB No.: 0970–0370.
Description: The federal Office of
Child Support Enforcement (OCSE),
Division of Federal Systems, maintains
the Child Support Portal (CSP), through
which authorized users may view,
update, or upload information for child
support purposes. To securely access
the Child Support Portal, authorized
users must complete a one-time CSP
registration form. OCSE uses
information collected at the time of
registration to verify the user’s
authorization to access the portal and to
establish a secure account.
The federal Child Support Portal
Registration information collection
activities are authorized by 42 U.S.C.
653(m)(2), which requires the Secretary
to establish and implement safeguards
to restrict access to confidential
information in the Federal Parent
Locator Service to authorized persons,
E:\FR\FM\22MYN1.SGM
22MYN1
23685
Federal Register / Vol. 83, No. 99 / Tuesday, May 22, 2018 / Notices
and to restrict use of such information
to authorized purposes.
Respondents: Employers, Financial
Institutions, Insurers, and Child Support
Agencies
ANNUAL BURDEN ESTIMATES
Information collection
instrument
Number of
respondents
Number of
responses per
respondent
Average
burden
hours per
response
Total burden
hours
Registration Screens .......................................................................................
648
1
0.15
97.20
Estimated Total Annual Burden
Hours: 97.20
In compliance with the requirements
of the Paperwork Reduction Act of 1995
(Pub. L. 104–13, 44 U.S.C. Chap 35), the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded 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. Email
address: infocollection@acf.hhs.gov. All
requests should be identified by the title
of the information collection.
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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2018–10910 Filed 5–21–18; 8:45 am]
amozie on DSK3GDR082PROD with NOTICES1
BILLING CODE 4184–41–P
VerDate Sep<11>2014
16:47 May 21, 2018
Jkt 241001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2018–N–1787]
Advisory Committee; Blood Products
Advisory Committee; Renewal
AGENCY:
Food and Drug Administration,
HHS.
Notice; renewal of advisory
committee.
ACTION:
The Food and Drug
Administration (FDA) is announcing the
renewal of the Blood Products Advisory
Committee by the Commissioner of
Food and Drugs (the Commissioner).
The Commissioner has determined that
it is in the public interest to renew the
Blood Products Advisory Committee for
an additional 2 years beyond the charter
expiration date. The new charter will be
in effect until May 13, 2020.
DATES: Authority for the Blood Products
Advisory Committee will expire on May
13, 2020, unless the Commissioner
formally determines that renewal is in
the public interest.
FOR FURTHER INFORMATION CONTACT:
Bryan Emery, Division of Scientific
Advisors and Consultants, Center for
Biologics Evaluation and Research,
Food and Drug Administration, 10993
New Hampshire Ave., Bldg. 71, Rm.
6268, Silver Spring, MD 20993–0002,
240–402–8054, Bryan.emery@
fda.hhs.gov.
SUMMARY:
Pursuant
to 41 CFR 102–3.65 and approval by the
Department of Health and Human
Services pursuant to 45 CFR part 11 and
by the General Services Administration,
FDA is announcing the renewal of the
Blood Products Advisory Committee.
The committee is a discretionary
Federal advisory committee established
to provide advice to the Commissioner.
The Blood Products Advisory
Committee advises the Commissioner or
designee in discharging responsibilities
as they relate to helping to ensure safe
and effective drugs for human use and,
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00061
Fmt 4703
Sfmt 4703
as required, any other product for which
FDA has regulatory responsibility.
The Committee shall consist of a core
of 17 voting members including the
Chair. Members and the Chair are
selected by the Commissioner or
designee from among authorities
knowledgeable in the fields of clinical
and administrative medicine,
hematology, immunology, blood
banking, surgery, internal medicine,
biochemistry, engineering, biological
and physical sciences, biotechnology,
computer technology, statistics,
epidemiology, sociology/ethics, and
other related professions. Members will
be invited to serve for overlapping terms
of up to 4 years. Almost all non-Federal
members of this committee serve as
Special Government Employees. The
core of voting members may include one
technically qualified member, selected
by the Commissioner or designee, who
is identified with consumer interests
and is recommended by either a
consortium of consumer-oriented
organizations or other interested
persons. In addition to the voting
members, the Committee may include
one non-voting member who is
identified with industry interests.
The Commissioner or designee shall
have the authority to select members of
other scientific and technical FDA
advisory committees (normally not to
exceed 10 members) to serve
temporarily as voting members and to
designate consultants to serve
temporarily as voting members when:
(1) Expertise is required that is not
available among current voting standing
members of the Committee (when
additional voting members are added to
the Committee to provide needed
expertise, a quorum will be based on the
combined total of regular and added
members), or (2) to comprise a quorum
when, because of unforeseen
circumstances, a quorum is or will be
lacking. Because of the size of the
Committee and the variety in the types
of issues that it will consider, FDA may,
in connection with a particular
committee meeting, specify a quorum
that is less than a majority of the current
E:\FR\FM\22MYN1.SGM
22MYN1
Agencies
[Federal Register Volume 83, Number 99 (Tuesday, May 22, 2018)]
[Notices]
[Pages 23684-23685]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-10910]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects:
Title: Federal Child Support Portal Registration.
OMB No.: 0970-0370.
Description: The federal Office of Child Support Enforcement
(OCSE), Division of Federal Systems, maintains the Child Support Portal
(CSP), through which authorized users may view, update, or upload
information for child support purposes. To securely access the Child
Support Portal, authorized users must complete a one-time CSP
registration form. OCSE uses information collected at the time of
registration to verify the user's authorization to access the portal
and to establish a secure account.
The federal Child Support Portal Registration information
collection activities are authorized by 42 U.S.C. 653(m)(2), which
requires the Secretary to establish and implement safeguards to
restrict access to confidential information in the Federal Parent
Locator Service to authorized persons,
[[Page 23685]]
and to restrict use of such information to authorized purposes.
Respondents: Employers, Financial Institutions, Insurers, and Child
Support Agencies
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Information collection instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Registration Screens........................ 648 1 0.15 97.20
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 97.20
In compliance with the requirements of the Paperwork Reduction Act
of 1995 (Pub. L. 104-13, 44 U.S.C. Chap 35), the Administration for
Children and Families is soliciting public comment on the specific
aspects of the information collection described above. Copies of the
proposed collection of information can be obtained and comments may be
forwarded 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. Email
address: [email protected]. All requests should be identified
by the title of the information collection.
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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2018-10910 Filed 5-21-18; 8:45 am]
BILLING CODE 4184-41-P