Webinars >>FDA Audit
FDA Regulation of Dietary Supplement Imports into the US
In 2010, FDA published the final rule governing importing of all dietary supplements into the US. This rule consolidated the previous rules for GMP, documentation, packaging and labeling, ingredient testing, and adverse event reporting requirements. The rules describe in great details the import and marketing requirements for all dietary supplements prior to import into the country or getting into US market, if manufactured domestically. Additional requirements such as Foreign Supplier Verification Program (FSVP) and third-party audit program have been proposed to further regulate the import of dietary supplements into the US.
This seminar will provide practical instructions to meet the current requirements in the process of manufacture and import of dietary supplements including description of key terms, concepts, and common issues that dietary supplement manufacturers are likely to encounter.
Why should you attend:
This seminar is intended for manufacturers and importers of dietary supplements who wish to have a better understanding of how FDA regulates dietary supplements and the custom clearance requirements for such products. Attendees will be introduced to the various rules that apply to dietary supplements and how to navigate the Customs entry process. Attending this training will help you to better manage your import compliance activities and help support your logistics supply chain.
Areas Covered in the Session:
Who will benefit:
The following individuals or disciplines will benefit from attending this Webinar:
For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: firstname.lastname@example.org