Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Manufactured Food Regulatory Program Standards, 41802-41803 [2013-16620]
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41802
Federal Register / Vol. 78, No. 133 / Thursday, July 11, 2013 / Notices
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
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. 2013–16643 Filed 7–10–13; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0115]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Manufactured
Food Regulatory Program Standards
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by August 12,
2013.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0601. Also
include the FDA docket number found
in brackets in the heading of this
document.
SUMMARY:
Ila
S. Mizrachi, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
7726, Ila.Mizrachi@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
FOR FURTHER INFORMATION CONTACT:
Manufactured Food Regulatory
Program Standards—(OMB Control
Number 0910–0601)—Extension
In the Federal Register of July 20,
2006 (71 FR 41221), FDA announced the
availability of a draft document entitled
‘‘Manufactured Food Regulatory
Program Standards (MFRPS).’’ These
draft program standards are the
framework that States should use to
design and manage its manufactured
food program. The implementation of
the standards will be negotiated as an
option for payment under the State food
contract. States that are awarded this
option will receive up to $25,000 over
a period of 5 years to fully implement
the program standards. Additionally, 26
States may receive up to $300,000 each
year for a period of 5 years to be in
compliance with the 10 standards.
In the first year of implementing the
program standards, the State program
conducts a baseline self-assessment to
determine if they meet the elements of
each standard. The State program
should use the worksheets and forms
contained herein; however, it can use
alternate forms that are equivalent. The
State program maintains the documents
and verifying records required for each
standard. The information contained in
the documents must be current and fitfor-use. If the State program fails to meet
all program elements and
documentation requirements of a
standard, it develops a strategic plan
which includes the following: (1) The
individual element of documentation
requirement of the standard that was not
met; (2) improvements needed to meet
the program element or documentation
requirement of the standard; and (3)
projected completion dates for each
task.
In the Federal Register of February
19, 2013 (78 FR 11651), FDA published
a 60-day notice requesting public
comment on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
Respondent
Number of
respondents
Number of
responses per
respondent
Total annual
responses
Average
burden per
response
Total hours
State Departments of Agriculture or Health ........................
44
1
44
303
13,332
emcdonald on DSK67QTVN1PROD with NOTICES
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
The burden has been calculated to
303 hours per respondent. This burden
was determined by capturing the
average amount of time for each
respondent to assess the current state of
the program and work toward
VerDate Mar<15>2010
18:23 Jul 10, 2013
Jkt 229001
implementation of each of the 10
standards contained in MFRPS. The
hours per respondent will remain the
same as implementation to account for
continuing improvement and selfsufficiency in the program.
PO 00000
Frm 00022
Fmt 4703
Sfmt 4703
Dated: July 5, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013–16620 Filed 7–10–13; 8:45 am]
BILLING CODE 4160–01–P
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Federal Register / Vol. 78, No. 133 / Thursday, July 11, 2013 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0001]
Orthopaedic and Rehabilitation
Devices Panel of the Medical Devices
Advisory Committee; Cancellation
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The meeting of the
Orthopaedic and Rehabilitation Devices
Panel of the Medical Devices Advisory
Committee scheduled for July 24 and
25, 2013, is cancelled. This meeting was
announced in the Federal Register of
April 25, 2013 (78 FR 24426).
FOR FURTHER INFORMATION CONTACT: Sara
J. Anderson, Center for Devices and
Radiological Health, Food and Drug
Administration,10903 New Hampshire
Ave., Bldg. 66, rm. 1611, Silver Spring,
MD 20993, 301–796–7047,
Sara.Anderson@fda.hhs.gov, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area), and follow the
prompts to the desired center or product
area. Please call the Information Line for
up-to-date information on this meeting.
SUMMARY:
Dated: July 5, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013–16621 Filed 7–10–13; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0757]
Establishment of a Public Docket for
Comment on the Report Prepared
Under the Food and Drug
Administration Safety and Innovation
Act Section 1138
AGENCY:
Food and Drug Administration,
HHS.
Establishment of docket; request
for comments.
emcdonald on DSK67QTVN1PROD with NOTICES
ACTION:
The Food and Drug
Administration (FDA) is announcing the
establishment of a public docket for
comments pertaining to the report
SUMMARY:
VerDate Mar<15>2010
18:23 Jul 10, 2013
Jkt 229001
mandated under the Food and Drug
Administration Safety and Innovation
Act (FDASIA) Section 1138, enacted
July 9, 2012, and posted on the FDA
Web site on July 9, 2013. This docket is
intended to solicit input on this report
from all relevant stakeholders.
DATES: Submit electronic or written
comments by September 9, 2013.
ADDRESSES: Submit electronic
comments to https://
www.regulations.gov. Submit written
comments to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Jonca Bull, Office of Minority Health,
Food and Drug Administration, 10903
New Hampshire Ave., Bldg. 32, rm.
4274, Silver Spring, MD 20993–0002,
301–796–8000, email:
jonca.bull@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
On July 9, 2012, President Obama
signed FDASIA (Pub. L. 112–144) into
law. Section 1138 of FDASIA requires
that FDA review and modify, as
necessary, the FDA communication plan
to inform and educate health care
providers and patients on the benefits
and risks of medical products, with
particular focus on underrepresented
subpopulations, including racial
subgroups.
Section 1138 of FDASIA requires that
FDA shall publicly post the
communication plan on the Internet
Web site of the Office of Minority
Health of FDA, and provide links to any
other appropriate Internet Web site, and
seek public comment on the
communication plan.
FDA is opening a docket for 60 days
to solicit input from all relevant
stakeholders regarding the
communication plan and Internet links.
This docket is intended to ensure that
stakeholders have an opportunity to
provide comments for further
improvements to the plan.
II. Comments
Interested persons may submit either
electronic comments regarding this
document to https://www.regulations.gov
or written comments to the Division of
PO 00000
Frm 00023
Fmt 4703
Sfmt 4703
41803
Dockets Management (see ADDRESSES). It
is only necessary to send one set of
comments. Identify comments with the
docket number found in brackets in the
heading of this document. Received
comments will be posted to the docket
at https://www.regulations.gov and may
be seen in the Division of Dockets
Management between 9 a.m. and 4 p.m.,
Monday through Friday.
Dated: July 5, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013–16617 Filed 7–10–13; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF JUSTICE
Notice of Lodging of Proposed
Amendment to Consent Decree Under
the Clean Water Act
On July 5, 2013, the Department of
Justice lodged a proposed amendment to
a consent decree with the United States
District Court for the Eastern District of
Missouri in the lawsuit entitled in
United States, et al. v. Metropolitan St.
Louis Sewer District, Civil Action No.
4:07–CV–01120.
Under the original 2012 consent
decree, the Metropolitan St. Louis
Sewer District (‘‘MSD’’) agreed to
undertake numerous measures to come
into compliance with the Clean Water
Act, including constructing and
implementing specific combined sewer
overflow control measures. MSD still is
in the process of complying with the
2012 decree. However, the proposed
amendment would replace two CSO
control measures (a treatment facility
and a local storage facility) as required
by the 2012 decree with one single CSO
storage facility.
The publication of this notice opens
a period of public comment on the
proposed amendment. Comments
should be addressed to the Assistant
Attorney General, Environment and
Natural Resources Division, and should
refer to United States, et al. v.
Metropolitan St. Louis Sewer District,
D.J. Ref. No. 90–5–1–1–08111. All
comments must be submitted no later
than thirty (30) days after the
publication date of this notice.
Comments may be submitted either by
email or by mail:
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Agencies
[Federal Register Volume 78, Number 133 (Thursday, July 11, 2013)]
[Notices]
[Pages 41802-41803]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-16620]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2013-N-0115]
Agency Information Collection Activities; Submission for Office
of Management and Budget Review; Comment Request; Manufactured Food
Regulatory Program Standards
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
proposed collection of information has been submitted to the Office of
Management and Budget (OMB) for review and clearance under the
Paperwork Reduction Act of 1995.
DATES: Fax written comments on the collection of information by August
12, 2013.
ADDRESSES: To ensure that comments on the information collection are
received, OMB recommends that written comments be faxed to the Office
of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer,
FAX: 202-395-7285, or emailed to oira_submission@omb.eop.gov. All
comments should be identified with the OMB control number 0910-0601.
Also include the FDA docket number found in brackets in the heading of
this document.
FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, Office of Information
Management, Food and Drug Administration, 1350 Piccard Dr., PI50-400B,
Rockville, MD 20850, 301-796-7726, Ila.Mizrachi@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has
submitted the following proposed collection of information to OMB for
review and clearance.
Manufactured Food Regulatory Program Standards--(OMB Control Number
0910-0601)--Extension
In the Federal Register of July 20, 2006 (71 FR 41221), FDA
announced the availability of a draft document entitled ``Manufactured
Food Regulatory Program Standards (MFRPS).'' These draft program
standards are the framework that States should use to design and manage
its manufactured food program. The implementation of the standards will
be negotiated as an option for payment under the State food contract.
States that are awarded this option will receive up to $25,000 over a
period of 5 years to fully implement the program standards.
Additionally, 26 States may receive up to $300,000 each year for a
period of 5 years to be in compliance with the 10 standards.
In the first year of implementing the program standards, the State
program conducts a baseline self-assessment to determine if they meet
the elements of each standard. The State program should use the
worksheets and forms contained herein; however, it can use alternate
forms that are equivalent. The State program maintains the documents
and verifying records required for each standard. The information
contained in the documents must be current and fit-for-use. If the
State program fails to meet all program elements and documentation
requirements of a standard, it develops a strategic plan which includes
the following: (1) The individual element of documentation requirement
of the standard that was not met; (2) improvements needed to meet the
program element or documentation requirement of the standard; and (3)
projected completion dates for each task.
In the Federal Register of February 19, 2013 (78 FR 11651), FDA
published a 60-day notice requesting public comment on the proposed
collection of information. No comments were received.
FDA estimates the burden of this collection of information as
follows:
Table 1--Estimated Annual Reporting Burden \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
Respondent Number of responses per Total annual Average burden Total hours
respondents respondent responses per response
--------------------------------------------------------------------------------------------------------------------------------------------------------
State Departments of Agriculture or Health......................... 44 1 44 303 13,332
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
The burden has been calculated to 303 hours per respondent. This
burden was determined by capturing the average amount of time for each
respondent to assess the current state of the program and work toward
implementation of each of the 10 standards contained in MFRPS. The
hours per respondent will remain the same as implementation to account
for continuing improvement and self-sufficiency in the program.
Dated: July 5, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013-16620 Filed 7-10-13; 8:45 am]
BILLING CODE 4160-01-P