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Who Should Attend: VPs, senior directors, and team members in CMC, QA, technical operations, and clinical development interested in the shift in manufacturing to non-US/EU facilities.

What You'll Learn: Join us for this interactive presentation to learn more about changes to laws governing the import of clinical trial supplies into the US and best practices for overcoming hurdles. Topics will include:

  • Changing interpretation of US importation laws
  • Obtaining an IND without clinical supplies
  • Impact on cost and timelines
  • Consequences of import refusal
  • Required importation documents
  • Recommended approach


  • Nikolas Burlew
    Vice President of Quality Systems, Clinipace Worldwide

Free Webcast:

Outsourcing Clinical Supplies Manufacturing: Navigating US Import Laws

Watch the webcast today!