Federal Register / Vol. 78, No.

33 / Tuesday, February 19, 2013 / Proposed Rules

must also be determined. Loads must be
determined for critical fuel and payload
distributions and centers of gravity.
Nose gear loads, as well as airframe
loads, must be determined. The airplane
must support these loads as described in
25.305.
Issued in Renton, Washington, on February
12, 2013.
Ali Bahrami,
Manager, Transport Airplane Directorate,
Aircraft Certification Service.

FOR FURTHER INFORMATION CONTACT:

BILLING CODE 491013P

Domini Bean, Office of Information

Management, Food and Drug
Administration, 1350 Picard Dr., PI50
400T, Rockville, MD 20850,
Domini.Bean@fda.hhs.gov.

DEPARTMENT OF HEALTH AND

HUMAN SERVICES

SUPPLEMENTARY INFORMATION:

[FR Doc. 201303679 Filed 21513; 8:45 am]

I. Background

Food and Drug Administration

21 CFR Parts 1, 16, 106, 110, 114, 117,
120, 123, 129, 179, and 211
[Docket No. FDA2011N0920]
RIN 0910AG36

Current Good Manufacturing Practice

and Hazard Analysis and Risk-Based
Preventive Controls for Human Food;
Extension of Comment Period for
Information Collection Provisions
AGENCY:

Food and Drug Administration,

HHS.
Proposed rule; extension of
comment period for information
collection provisions.

ACTION:

The Food and Drug

Administration (FDA or we) is
extending the comment period for the
information collection related to the
proposed rule on Current Good
Manufacturing Practice and Hazard
Analysis and Risk-Based Preventive
Controls for Human Food that
appeared in the Federal Register of
January 16, 2013. In the preamble to the
proposed rule, FDA requested
comments on the information collection
provisions that are subject to review by
the Office of Management and Budget
(OMB) under the Paperwork Reduction
Act of 1995. We are taking this action
in response to requests for an extension
to allow interested persons additional
time to submit comments on the
information collection provisions
associated with the rule.
DATES: The comment period for the
proposed rule published January 16,
2013 (78 FR 3646), is extended. Submit
either electronic or written comments
by May 16, 2013.
ADDRESSES: To ensure that comments on
information collection are received,
OMB recommends that written
SUMMARY:

srobinson on DSK4SPTVN1PROD with PROPOSALS

comments be faxed to the Office of

Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
2023957285, or emailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
title Current Good Manufacturing
Practice and Hazard Analysis and RiskBased Preventive Controls for Human
Food.

VerDate Mar<15>2010

16:48 Feb 15, 2013

Jkt 229001

In the Federal Register of January 16,

2013 (78 FR 3646), FDA published a
proposed rule entitled Current Good
Manufacturing Practice and Hazard
Analysis and Risk-Based Preventive
Controls for Human Food with a 120day comment period on the provisions
of the proposed rule and a 30-day
comment period on the information
collection provisions that are subject to
review by OMB under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501
3520). Comments on the provisions of
the rule and on the information
collection provisions will inform FDAs
rulemaking to modernize the regulation
for Current Good Manufacturing
Practice In Manufacturing, Packing, or
Holding Human Food and to add
requirements for domestic and foreign
facilities that are required to register
under the Federal Food, Drug, and
Cosmetic Act to establish and
implement hazard analysis and riskbased preventive controls for human
food.
OMB and FDA have received two
requests for a 90-day extension of the
comment period for the information
collection provisions of the proposed
rule. The requests conveyed concern
that the current 30-day comment period
does not allow sufficient time to
develop a meaningful or thoughtful
response to the information collection
provisions submitted to OMB under the
Paperwork Reduction Act of 1995.
We have considered the requests and
are extending the comment period for
the information collection for 90 days,
until May 16, 2013. We believe that a
90-day extension allows adequate time
for interested persons to submit
comments without significantly
delaying rulemaking on these important
issues. A 90-day extension also will
make the comment period for the
information collection provisions the

PO 00000

Frm 00008

Fmt 4702

Sfmt 4702

11611

same as the comment period for the

provisions of the proposed rule.
II. Request for Comments
Interested persons may either submit
electronic comments regarding the
information collection to
oira_submission@omb.eop.gov or fax
written comments to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
2023957285. All comments should be
identified with the title Current Good
Manufacturing Practice and Hazard
Analysis and Risk-Based Preventive
Controls for Human Food.
Dated: February 13, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 201303732 Filed 21513; 8:45 am]
BILLING CODE 416001P

DEPARTMENT OF HEALTH AND

HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 16 and 112
[Docket No. FDA2011N0921]
RIN 0910AG35

Standards for the Growing, Harvesting,

Packing, and Holding of Produce for
Human Consumption; Extension of
Comment Period for Information
Collection Provisions
AGENCY:

Food and Drug Administration,

HHS.
Proposed rule; extension of
comment period for information
collection provisions.

ACTION:

The Food and Drug

Administration (FDA or we) is
extending the comment period for the
information collection provisions of the
proposed rule on Standards for the
Growing, Harvesting, Packing, and
Holding of Produce for Human
Consumption that appeared in the
Federal Register of January 16, 2013. In
the preamble to the proposed rule, FDA
requested comments on the information
collection provisions that are subject to
review by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995. We are taking
this action in response to requests for an
extension to allow interested persons
additional time to submit comments on
the information collection provisions
associated with the rule.
DATES: The comment period for the
proposed rule published January 16,
2013 (78 FR 3504), is extended. Submit
SUMMARY:

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19FEP1