Webinars >>FDA Regulations
Export of FDA Regulated Products from US to Other countries: Export Certificates and Other Documents

FDA issues about 7 different kinds of export certificates for products intended to the exported from the US to other countries. These certificates are needed for the importing country; without such certificates these products will not be allowed entry into the importing country. Many companies export not only products marketed in the US but also products that may not be legally marketed in the US but are allowed in other countries. For exporters of drugs, biologics, medical devices, diagnostics, food, and all other kinds products or components it is important to have an understanding of the documentation requirements, application process, expectations of the FDA, and the importing country to avoid delays due to custom clearance. Before FDA can issue an export certificate to a company, it requires detailed compliance documents and other paperwork from the applicant. Incomplete and inaccurate documents is the most common reason for delays and denials of export certificates.

This seminar will provide practical instructions in the process of getting export certificates from FDA including description of key terms, concepts, and common issues that exporters of FDA-regulated products are likely to encounter.  
Why should you atte​nd:
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This seminar is intended for exporters of FDA regulated products or those that sell regulated products to U.S. exporters and wish to have a better understanding of how FDA regulated products are exported from the U.S. Attendees will be introduced to the types of export certificates, conditions under which FDA issues or denies export certificates, legal requirements, fees, and regulatory requirements for export of FDA-regulated products from the US. Attending this training will help you to better manage your export compliance activities and help support your logistics supply chain.
Areas Covered in the Session:
  • FDA export certificate issuance process
  • US Customs export documentation requirements
  • FDA export product codes
  • Regulatory requirements for exported products
  • Prior Notice process
  • Role of US agent for exports
  • Dealing with refusal to issue export certificates
Who will benefit:

The following individuals or disciplines will benefit from attending this Webinar:
  • Exporters of FDA regulated products to other countries
  • Foreign exporters and importers of FDA regulated products (companies which buy regulated products for non-U.S. sales)
  • Compliance officers
  • Logistics/Supply chain managers and analysts
  • Trade regulatory/legislative affairs professionals
  • Sales/marketing personnel
  • International business operations
  • Customs or Trade Compliance Personnel or Officers
  • Export or Global Trade Directors or Managers
  • Export Supervisors
  • Customs Brokers
  • Companies interested in exporting US products to other countries for sales and reprocessing
Date: On-Demand
Time: 12 PM ET        
​Duration: 60 Minutes

Speaker
Mukesh Kumar, PhD, RAC
Brij Strategic Consultations,
USA
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    For more info, fill the box below. We will contact you within 24 hrs.
For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: info@fdamap.com