Submission for OMB Review; Comment Request, 41543-41544 [2016-15046]
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41543
Federal Register / Vol. 81, No. 123 / Monday, June 27, 2016 / Notices
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2016–15116 Filed 6–24–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: ACF–OGM–PPR-Form B—
Program Indicators.
OMB No.: 0970–0406.
Description: The Office of Grants
Management (OGM), in the
Administration for Children and
families (ACF) is proposing the
collection of program performance data
for ACF’s discretionary grantees. To
collect this data OGM has developed a
form from the basic template of the
OMB-approved reporting format of the
Program Performance Report. OGM will
use this data to determine if grantees are
proceeding in a satisfactory manner in
meeting the approved goals and
objectives of the project, and if funding
should be continued for another budget
period.
The requirement for grantees to report
on performance is OMB grants policy.
Specific citations are contained in: (1) 2
CFR 215 Uniform Administrative
Requirements, cost Principles, and
Audit Requirements for Federal Awards
and (2) 45 CFR 75, Uniform
Administrative Requirements, Cost
Principles, and Audit Requirements for
Department of Health and Human
Services Awards.
Respondents: All ACF Discretionary
Grantees. State governments, Native
American Tribal governments, Native
American Tribal Organizations, Local
Governments, and Nonprofits with or
without 501 (c)(3) status with the IRS.
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
ACF–OGM–PPR–B .........................................................................................
6000
1
1
6000
Estimated Total Annual Burden
Hours: 6000.
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, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. All requests should be
identified by the 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 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. 2016–15094 Filed 6–24–16; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: National Medical Support
Notice
OMB No.: 0970–0222
Description: The National Medical
Support Notice (NMSN) is a two-part
document that requires information
from State child support enforcement
agencies, employers, and health plan
administrators to assist in enforcing
health care coverage provisions in a
child support order. The Department of
Health and Human Services (DHHS),
Administration for Children and
Families (ACF) developed and
maintains part A of the NMSN, which
is sent to an obligor’s employer for
completion; the Department of Labor
(DOL) developed and maintains part B
of the NMSN, which is provided to
health care administrators following
completion of part A.
DOL revised part B to conform with
changes to the currently approved part
A and is seeking a three-year approval
from OMB. To avoid burdening the
State child support enforcement
agencies with potential reprogramming
at varying times due to future changes
in part A or B, ACF is resubmitting an
unchanged information collection
package and requesting an extension to
the current OMB approval of NMSN
part A to synchronize the expiration
date with NMSN part B.
Respondents: State child support
enforcement agencies, employers, and
health plan administrators.
ANNUAL BURDEN ESTIMATES
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Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total
burden hours
National Medical Support Notice–Part A .........................................................
54
76,499
.17 hours
702,261
Estimated Total Annual Burden
Hours: 702,261.
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Additional Information: Copies of the
proposed collection may be obtained by
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writing to the Administration for
Children and Families, Office of
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Federal Register / Vol. 81, No. 123 / Monday, June 27, 2016 / Notices
Planning, Research and Evaluation, 330
C Street SW., Washington, DC 20201.
Attention Reports Clearance Officer. All
requests should be identified by the 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 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.
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 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’’).
Robert Sargis,
Reports Clearance Officer.
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Division of
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Division of Dockets
Management, 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–
2016–D–1174 for ‘‘Special Protocol
Assessment; Draft Guidance for
Industry.’’ Received comments will be
placed in the docket and, except for
those submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Division of Dockets Management
between 9 a.m. and 4 p.m., Monday
through Friday.
• 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
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on https://
[FR Doc. 2016–15046 Filed 6–24–16; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2016–D–1174]
Special Protocol Assessment; Draft
Guidance for Industry; Extension of
the Comment Period
AGENCY:
Food and Drug Administration,
HHS.
Notice; extension of the
comment period.
ACTION:
The Food and Drug
Administration (FDA or we) is
extending the comment period for the
notice of availability, published in the
Federal Register of May 4, 2016 (81 FR
26799), announcing the draft guidance
for industry entitled ‘‘Special Protocol
Assessment.’’ We are taking this action
due to maintenance on the Federal
eRulemaking portal from July 1 through
July 5, 2016.
DATES: Submit either electronic or
written comments by July 19, 2016.
ADDRESSES: You may submit comments
as follows:
SUMMARY:
mstockstill on DSK3G9T082PROD with NOTICES
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
VerDate Sep<11>2014
18:52 Jun 24, 2016
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www.regulations.gov. Submit both
copies to the Division of Dockets
Management. If you do not wish your
name and contact information to be
made publicly available, you can
provide this information on the cover
sheet and not in the body of your
comments and you must identify this
information as ‘‘confidential.’’ Any
information marked as ‘‘confidential’’
will not be disclosed except in
accordance with 21 CFR 10.20 and other
applicable disclosure law. For more
information about FDA’s posting of
comments to public dockets, see 80 FR
56469, September 18, 2015, or access
the information at: https://www.fda.gov/
regulatoryinformation/dockets/
default.htm.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Amalia Himaya, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 22, Rm. 6439,
Silver Spring, MD 20993–0002, 301–
796–0700; or Stephen Ripley, Center for
Biologics Evaluation and Research,
Food and Drug Administration, 10903
New Hampshire Ave., Bldg. 71, Rm.
3128, Silver Spring, MD 20993–0002,
240–402–7911.
In the
Federal Register of May 4, 2016 (81 FR
26799), FDA published a notice of
availability.
Interested persons were originally
given until July 5, 2016, to comment on
the draft guidance for industry entitled
‘‘Special Protocol Assessment.’’
From July 1 through July 5, 2016, the
Federal eRulemaking Portal, https://
www.regulations.gov, is undergoing
maintenance. We are, therefore,
extending the comment period for the
draft guidance for industry entitled
‘‘Special Protocol Assessment.’’ The
extended comment period will close on
July 19, 2016.
SUPPLEMENTARY INFORMATION:
Dated: June 21, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016–15106 Filed 6–24–16; 8:45 am]
BILLING CODE 4164–01–P
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[Federal Register Volume 81, Number 123 (Monday, June 27, 2016)]
[Notices]
[Pages 41543-41544]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-15046]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: National Medical Support Notice
OMB No.: 0970-0222
Description: The National Medical Support Notice (NMSN) is a two-
part document that requires information from State child support
enforcement agencies, employers, and health plan administrators to
assist in enforcing health care coverage provisions in a child support
order. The Department of Health and Human Services (DHHS),
Administration for Children and Families (ACF) developed and maintains
part A of the NMSN, which is sent to an obligor's employer for
completion; the Department of Labor (DOL) developed and maintains part
B of the NMSN, which is provided to health care administrators
following completion of part A.
DOL revised part B to conform with changes to the currently
approved part A and is seeking a three-year approval from OMB. To avoid
burdening the State child support enforcement agencies with potential
reprogramming at varying times due to future changes in part A or B,
ACF is resubmitting an unchanged information collection package and
requesting an extension to the current OMB approval of NMSN part A to
synchronize the expiration date with NMSN part B.
Respondents: State child support enforcement agencies, employers,
and health plan administrators.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
National Medical Support Notice-Part A...... 54 76,499 .17 hours 702,261
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 702,261.
Additional Information: Copies of the proposed collection may be
obtained by writing to the Administration for Children and Families,
Office of
[[Page 41544]]
Planning, Research and Evaluation, 330 C Street SW., Washington, DC
20201. Attention Reports Clearance Officer. All requests should be
identified by the 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 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. 2016-15046 Filed 6-24-16; 8:45 am]
BILLING CODE 4184-01-P
