[Federal Register Volume 78, Number 220 (Thursday, November 14, 2013)]
[Notices]
[Page 68460]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2013-27213]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2013-D-0880]
Draft Guidance for Industry on Frequently Asked Questions About
Medical Foods; Second Edition; Reopening of the Comment Period
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice; reopening of the comment period.
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SUMMARY: The Food and Drug Administration (FDA or we) is reopening the
comment period for the draft guidance for industry entitled
``Frequently Asked Questions About Medical Foods; Second Edition.'' We
are reopening the comment period in response to requests for an
extension to allow interested persons additional time to submit
comments.
DATES: Submit either electronic or written comments by December 16,
2013.
ADDRESSES: Submit electronic comments on the draft guidance to http://www.regulations.gov.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.
FOR FURTHER INFORMATION CONTACT: Shawne Suggs-Anderson, Center for Food
Safety and Applied Nutrition (HFS-850), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park, MD 20740, 240-402-1783.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of August 13, 2013 (78 FR 49271), we
published a notice announcing the availability of an updated draft
guidance for industry entitled ``Frequently Asked Questions About
Medical Foods; Second Edition.'' (We had published earlier versions of
the guidance in May 1997 and May 2007.) The draft guidance, when
finalized, will update some responses to questions that appeared in
earlier versions of the guidance and add new questions and responses
regarding the definition, labeling, and availability of medical foods.
We invited comment on the draft guidance by October 15, 2013.
II. Request for Comments
Following publication of the August 13, 2013, notice of
availability, we received requests for a 60-day extension of the
comment period. The requesters explained that they needed more time to
review the guidance, develop comments, and assemble data.
If all of the guidance in the August 13, 2013, version were new, a
reopening of the comment period for 60 additional days might be
warranted. However, much of the draft guidance remains unchanged from
our last revision in 2007. The additional content focuses on FDA's
thinking relating to use of medical foods under supervision by a
physician, whether medical foods should be sold by prescription only,
and types of diseases and conditions that a medical food could be used
to manage. We are, therefore, reopening the comment period for the
draft guidance for an additional 30 days, until December 16, 2013. We
believe that this reopening allows adequate time for interested persons
to submit comments without significantly delaying further FDA action on
this draft guidance. (We initially intended to extend the comment
period, but, due to the lapse in appropriations and resulting cessation
of many government operations from October 1 through October 16, 2013,
we were unable to issue a notice extending the comment period before
October 15, 2013; consequently, we are reopening the comment period for
an additional 30 days.)
III. How To Submit Comments
Interested persons may submit either electronic comments regarding
the draft guidance to http://www.regulations.gov or written comments to
the Division of 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 may be seen in the Division of Dockets Management
between 9 a.m. and 4 p.m., Monday through Friday, and may be posted to
the docket at http://www.regulations.gov.
Dated: November 7, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013-27213 Filed 11-13-13; 8:45 am]
BILLING CODE 4160-01-P