Submission for OMB Review; Comment Request, 25298 [2015-10296]
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25298
Federal Register / Vol. 80, No. 85 / Monday, May 4, 2015 / 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.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2015–10286 Filed 5–1–15; 8:45 am]
Submission for OMB Review;
Comment Request
BILLING CODE 4163–18–P
Administration for Children and
Families
Title: Child Care Development Fund,
CCDF; Reporting Improper Payments;
Instructions for States.
OMB No.: 0970–0323.
Description: Section 2 of the Improper
Payments Act of 2002 provides for
estimates and reports of improper
payments by Federal agencies. Subpart
K of 45 CFR, part 98 will require States
to prepare and submit a report of errors
occurring in the administration of CCDF
grant funds once every three years.
The Office of Child Care (OCC) is
completing the third 3-year cycle of case
record reviews to meet the requirements
for reporting under IPIA. The current
forms and instructions expire
September 30, 2015. OCC is submitting
the information collection for renewal
clearance with minor changes.
Responders will now have additional
guidance and clarification in the
instructions and errors have been
corrected. New language incorporates
requirements from the 2014 Child Care
and Development Fund Block Grant Act
passed in November 2014.
Respondents: State grantees, the
District of Columbia, and Puerto Rico
ANNUAL BURDEN ESTIMATES
mstockstill on DSK4VPTVN1PROD with NOTICES
Sampling Decisions and Fieldwork Preparation Plan .................
Record Review Worksheet ..........................................................
State Improper Authorizations for Payment Report ....................
Corrective Action Plan .................................................................
Estimated Total Annual Burden
Hours: 43,613.36.
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. 2015–10296 Filed 5–1–15; 8:45 am]
BILLING CODE 4184–01–P
VerDate Sep<11>2014
19:40 May 01, 2015
Jkt 235001
Number of
responses per
respondent
Number of
respondents
Instrument
17
17
17
8
1
276
1
1
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–E–0785]
Determination of Regulatory Review
Period for Purposes of Patent
Extension; RELAY THORACIC STENT–
GRAFT WITH PLUS DELIVERY
SYSTEM
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) has determined
the regulatory review period for the
RELAY THORACIC STENT–GRAFT
WITH PLUS DELIVERY SYSTEM and is
publishing this notice of that
determination as required by law. FDA
has made the determination because of
the submission of an application to the
Director of the U.S. Patent and
Trademark Office (USPTO), Department
of Commerce, for the extension of a
patent which claims that medical
device.
SUMMARY:
Submit electronic
comments to https://
www.regulations.gov. Submit written
petitions (two copies are required) and
written comments to the Division of
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
ADDRESSES:
PO 00000
Frm 00025
Fmt 4703
Sfmt 4703
Average burden
hours per
response
106
6.33
639
156
Total burden
hours
1,802
29,700.36
10,863
1,248
Lane, Rm. 1061, Rockville, MD 20852.
Submit petitions electronically to https://
www.regulations.gov at Docket No.
FDA–2013–S–0610.
FOR FURTHER INFORMATION CONTACT:
Beverly Friedman, Office of
Management, Food and Drug
Administration, 10001 New Hampshire
Ave., Hillandale Campus, Rm. 3180,
Silver Spring, MD 20993, 301–796–
7900.
SUPPLEMENTARY INFORMATION: The Drug
Price Competition and Patent Term
Restoration Act of 1984 (Pub. L. 98–417)
and the Generic Animal Drug and Patent
Term Restoration Act (Pub. L. 100–670)
generally provide that a patent may be
extended for a period of up to 5 years
so long as the patented item (human
drug product, animal drug product,
medical device, food additive, or color
additive) was subject to regulatory
review by FDA before the item was
marketed. Under these acts, a product’s
regulatory review period forms the basis
for determining the amount of extension
an applicant may receive.
A regulatory review period consists of
two periods of time: A testing phase and
an approval phase. For medical devices,
the testing phase begins with a clinical
investigation of the device and runs
until the approval phase begins. The
approval phase starts with the initial
submission of an application to market
the device and continues until
permission to market the device is
E:\FR\FM\04MYN1.SGM
04MYN1
Agencies
[Federal Register Volume 80, Number 85 (Monday, May 4, 2015)]
[Notices]
[Page 25298]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-10296]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Child Care Development Fund, CCDF; Reporting Improper
Payments; Instructions for States.
OMB No.: 0970-0323.
Description: Section 2 of the Improper Payments Act of 2002
provides for estimates and reports of improper payments by Federal
agencies. Subpart K of 45 CFR, part 98 will require States to prepare
and submit a report of errors occurring in the administration of CCDF
grant funds once every three years.
The Office of Child Care (OCC) is completing the third 3-year cycle
of case record reviews to meet the requirements for reporting under
IPIA. The current forms and instructions expire September 30, 2015. OCC
is submitting the information collection for renewal clearance with
minor changes. Responders will now have additional guidance and
clarification in the instructions and errors have been corrected. New
language incorporates requirements from the 2014 Child Care and
Development Fund Block Grant Act passed in November 2014.
Respondents: State grantees, the District of Columbia, and Puerto
Rico
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Sampling Decisions and Fieldwork 17 1 106 1,802
Preparation Plan.....................
Record Review Worksheet............... 17 276 6.33 29,700.36
State Improper Authorizations for 17 1 639 10,863
Payment Report.......................
Corrective Action Plan................ 8 1 156 1,248
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 43,613.36.
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. 2015-10296 Filed 5-1-15; 8:45 am]
BILLING CODE 4184-01-P