98-33052. Announcement of a New Format for Export Certificates  

  • [Federal Register Volume 63, Number 239 (Monday, December 14, 1998)]
    [Notices]
    [Pages 68774-68775]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-33052]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket No. 98N-1063]
    
    
    Announcement of a New Format for Export Certificates
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
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    SUMMARY: The Food and Drug Administration (FDA) is announcing a new 
    format for export certificates. The new format features the use of 
    several security measures in the paper used to print export 
    certificates to deter falsification of or tampering with FDA-
    
    [[Page 68775]]
    
    issued export certificates. The new format may also help authenticate 
    export certificates.
    
    DATES: The agency will begin issuing export certificates using the new 
    format after January 1, 1999.
    
    FOR FURTHER INFORMATION CONTACT: Philip L. Chao, Office of Policy (HF-
    23), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 
    20857, 301-827-3380.
    
    SUPPLEMENTARY INFORMATION: Firms exporting products from the United 
    States are often asked by foreign customers or foreign governments to 
    supply a certification relating to products subject to the Federal 
    Food, Drug, and Cosmetic Act (the act) and other FDA-administered acts. 
    Certification is the process by which a formal or official attestation 
    is made concerning a product's regulatory status or the system by which 
    a commodity is manufactured. Certification does not show that FDA has 
    ``approved'' the product for export; however, some certificates reflect 
    that the product has been approved for marketing in the United States.
        FDA currently issues several types of certificates. In brief, the 
    principal certificates are:
        1. Certificates to Foreign Government--used for products that may 
    be legally marketed, sold, offered for sale, or distributed in the 
    United States. For food products, these are commonly known as 
    ``certificates of free sale'' or ``certificates of export.''
        2. Certificates of Exportability--used for products that meet the 
    requirements for export under section 801(e) or 802 of the act (21 
    U.S.C. 381(e) or 382)) but may not otherwise be marketed, sold, offered 
    for sale, or distributed in the United States.
        3. Certificates of a Pharmaceutical Product--used for 
    pharmaceutical products and conform to the format in the World Health 
    Organization's ``Certification Scheme on the Quality of Pharmaceutical 
    Products Moving in International Commerce.''
        FDA's Center for Biologics Evaluation and Research, Center for Drug 
    Evaluation and Research, Center for Devices and Radiological Health, 
    Center for Food Safety and Applied Nutrition, and Center for Veterinary 
    Medicine receive and process requests for export certificates for 
    products subject to their respective authorities.
        Recently, there has been an increasing demand for export 
    certificates, as well as requests from foreign governments to 
    authenticate certificates and instances where FDA has found counterfeit 
    or falsified certificates. Consequently, to facilitate the issuance and 
    tracking of export certificates, deter unscrupulous persons from making 
    counterfeit or false certificates or otherwise tampering with export 
    certificates, and to help foreign governments identify authentic, FDA-
    issued export certificates more readily, FDA has adopted a new format 
    for its export certificates. The new format features the use of several 
    security measures in the paper used for export certificates.
        FDA will begin using the new format on certificates issued after 
    January 1, 1999. The procedures for requesting and issuing export 
    certificates, as well as the text of the certificates themselves, will 
    remain unchanged.
        However, FDA will not use the new format on European Union (EU) 
    Export Health Certificates. These certificates are for fishery products 
    intended for import into the EU and are not considered to be FDA 
    certificates.
        FDA is notifying foreign embassies and its counterpart government 
    agencies of the new format and also advising them that otherwise valid 
    export certificates issued before January 1, 1999, remain valid. 
    Consequently, persons whose export certificates were issued before 
    January 1, 1999, but expire after that date, should not need to replace 
    those certificates.
    
        Dated: December 4, 1998.
    William K. Hubbard,
    Associate Commissioner for Policy Coordination.
    [FR Doc. 98-33052 Filed 12-11-98; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
12/14/1998
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
98-33052
Dates:
The agency will begin issuing export certificates using the new format after January 1, 1999.
Pages:
68774-68775 (2 pages)
Docket Numbers:
Docket No. 98N-1063
PDF File:
98-33052.pdf