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 Regulatory FAQ Database
 
About ITCI
Export Start-Up Kit
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Regulatory FAQs
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and Companies
Book - Roadmap To Export Success

 
    What if my product is a drug or medical device?

    If your product is considered a drug or a medical device under the law, your request will require review by FDA's Center for Drug Evaluation and Research (CDER) or FDA's Center for Devices and Radiological Health (CDRH). If you need additional information about exporting drugs, please contact CDER's Export Certificate Team at (301) 796-3217 or (301) 796-3218. If you need additional information about exporting medical devices, please contact CDRH at (240) 276-0132 or email exportcert@cdrh.fda.gov.

    U.S. Food and Drug Administration (FDA)
    http://www.fda.gov


 
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