About The Webinar

New requirements for cosmetics companies come into effect July 1 under the Modernization of Cosmetics Regulation Act. Every manufacturer of a cosmetic product distributed in the U.S. must register and may have to list its products with the Food and Drug Administration. Distributors may also be required to list the products they sell, depending on how the product is labeled. Failure to comply with this new law  and all its provisions (such as registration and good manufacturing practices) could result in detention or refusal of cosmetic import entries.

This 30-minute webinar will help importers, exporters, distributors, and manufacturers of cosmetic products better understand the major requirements of this new law.

Contact if you have issues registering. Please note we do not take American Express.

Key Topics

  • Understanding new terminology and how it could impact you as a manufacturer, distributor or retailer
  • Requirement for every cosmetic manufacturing facility to register with the FDA before July 1
  • Requirement for every foreign facility to designate a U.S. agent
  • New responsibilities and liabilities that come with accepting U.S. agent designation 
  • New GMP requirements

Please note we do not accept payment via American Express.


Domenic J. Veneziano

Independent FDA Regulatory and Strategic Consultant


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