[Federal Register: January 15, 2009 (Volume 74, Number 10)]
[Notices]
[Page 2600-2601]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr15ja09-111]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2004-D-0043] (formerly Docket No. 2004D-0510)
Guidance for Industry: Referral Program from the Food and Drug
Administration to the National Oceanic and Atmospheric Administration
Seafood Inspection Program for the Certification of Fish and Fishery
Products for Export to the European Union and the European Free Trade
Association; Availability
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is announcing the
availability of a guidance document entitled ``Guidance for Industry:
Referral Program from the Food and Drug Administration to the National
Oceanic and Atmospheric Administration Seafood Inspection Program for
the Certification of Fish and Fishery Products for Export to the
European Union and the European Free Trade Association.'' The guidance
provides information for seafood processors and other entities that are
interested in obtaining export certificates for fish or fishery
products that are to be shipped to the European Union (EU) and the
European Free Trade Association (EFTA). FDA is also announcing that it
intends to stop issuing EU Export Certificates after February 17, 2009.
DATES: Submit written or electronic comments on the guidance at any
time.
ADDRESSES: Submit written comments concerning the guidance to the
Division of Dockets Management (HFA-305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville, MD 20852. Submit electronic
comments on the guidance to http://www.regulations.gov. Submit written
requests for single copies of the guidance to the Office of Food Safety
(HFS-300), Center for Food Safety and Applied Nutrition, Food and Drug
Administration, 5100 Paint Branch Pkwy., College Park, MD 20740-3835.
Send one self-addressed adhesive label to assist that office in
processing your request. See the SUPPLEMENTARY INFORMATION section for
electronic access to the guidance.
FOR FURTHER INFORMATION CONTACT: William Jones, Center for Food Safety
and Applied Nutrition (HFS-325), Food and Drug Administration, 5100
Paint Branch Pkwy., College Park, MD 20740-3835, 301-436-2300.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of November 26, 2004 (69 FR 68948) (the
November 26 notice), FDA announced the availability of a draft guidance
entitled ``Proposed Referral Program from the Food and Drug
Administration to the National Oceanic and Atmospheric Administration
Seafood Inspection Program for the Certification of Live and Perishable
Fish and Fishery Products for Export to the European Union and the
European Free Trade Association.'' In the November 26 notice, FDA
announced that it proposed to operate a Referral Program for a 24-month
period to test the viability and effectiveness of such an arrangement.
During this period, EU Export Certificates for shipments of live and
perishable fish and fishery products destined for the EU, European
Union Accession Partnership Countries (EUAPC), and EFTA Members would
have been issued by the National Oceanic and Atmospheric Administration
Seafood Inspection Program (NOAA SIP) under the Agricultural Marketing
Act. In addition, FDA indicated that it intended to stop issuing EU
Export Certificates for live and perishable fish and fishery products
during this period. FDA sought comment on this referral program,
including whether it should be expanded beyond live and perishable to
all shipments of fish and fishery products destined for the EU, EU
Accession Partnership Countries, and other countries with certificate
requirements.
Interested persons were initially given until December 27, 2004, to
comment on the draft guidance. The comment period was subsequently
extended until January 25, 2005 (69 FR 78038, December 29, 2004). The
agency considered and modified the guidance as appropriate.
The agency is announcing the availability of the final guidance
document entitled ``Guidance for Industry: Referral Program from the
Food and Drug Administration to the National Oceanic and Atmosphere
Administration Seafood Inspection Program for the Certification of Fish
and Fishery Products for the Export to the European Union and the
European Free
[[Page 2601]]
Trade Association.'' In this final guidance, FDA is announcing that:
(1) We intend to proceed with a Certification Referral Program to NOAA
SIP, without a 24-month test period, (2) we intend to expand the
program to include all fish and fishery products for export to the EU
and EFTA, and (3) we intend to stop issuing EU Export Certificates
effective February 17, 2009. The agency intends to adopt this approach
because the industry's demand for EU Export Certificates continues to
rise dramatically, and FDA can no longer justify the use of our limited
food safety resources for issuance of EU Export Certificates. The
implementation of this guidance should free up resources that the
agency can allocate for higher priority public health activities that
are intended to protect the U.S. consuming public, while still
providing a mechanism for the industry to continue obtaining EU
certification. Seafood processors and other entities involved in the
exporting of seafood to the EU may obtain EU Export Certificates from
the NOAA SIP.
FDA is issuing this guidance document as a level 1 guidance
consistent with FDA's good guidance practices regulation (21 CFR
10.115). This guidance represents FDA's current thinking on this topic.
It does not create or confer any rights for or on any person and does
not operate to bind FDA, NOAA SIP, or the public. An alternative
approach may be used if such approach satisfies the requirements of the
applicable statutes and regulations.
II. Comments
Interested persons may submit to the Division of Dockets Management
(see ADDRESSES) written or electronic comments regarding this document.
Submit a single copy of electronic comments or two paper copies of any
mailed comments, except that individuals may submit one paper copy.
Comments are to be identified with the docket number found in brackets
in the heading of this document. The guidance and received comments may
be seen in the Division of Dockets Management between 9 a.m. and 4
p.m., Monday through Friday.
Please note that on January 15, 2008, the FDA Division of Dockets
Management Web site transitioned to the Federal Dockets Management
System (FDMS). FDMS is a Government-wide, electronic docket management
system. Electronic comments or submissions will be accepted by FDA only
through FDMS at http://www.regulations.gov.
III. Electronic Access
Persons with access to the Internet may obtain the guidance
document at http://www.cfsan.fda.gov/guidance.html.
Dated: January 9, 2009.
Jeffrey Shuren,
Associate Commissioner for Policy and Planning.
[FR Doc. E9-785 Filed 1-14-09; 8:45 am]
BILLING CODE 4160-01-S