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Foods, Supplements, Cosmetics, Devices…Oh My: How the FDA Regulates More Than You May Think!

Upon purchase, an email will be sent with login details. A few days after the live webinar, you will receive an email with a link to view the recording, a copy of the presentation, and a certificate of completion. Access to view the webinar recording will be available for one year from the purchase date.

The U.S. Food and Drug Administration (FDA) regulates the import, distribution, and sale of foods, dietary supplements, cosmetics, medical devices, radiation-emitting products, drugs, and animal and veterinary products. Practically everything we use day to day. The FDA is a unique organization – serving at the cusp of innovation, providing industry with guidelines on how to operate compliantly, and enforcing rules and taking action when needed. 

Understanding the categories and subcategories of items that are regulated, how they are regulated, and how to mitigate enforcement action is critical to ensuring the free flow of goods, increasing your bottom line, and ensuring consumer confidence. We’ll discuss in this webinar whether FDA has jurisdiction over your goods, what that means, how to be compliant with the product, across the supply chain and in marketing and advertising channels, and what the FDA importation process looks like.

This webinar will provide PowerPoint slides and include live video and commentary. Each registrant (even if you can’t attend the live event) will receive a copy of the presentation, certificate of completion, speaker contact information for follow-up questions, and access to the webinar recording a few days after the webinar airs. Webinar participants are invited to submit questions during the webinar and the final 30 minutes will be allotted to answering attendee questions.

 

Speaker Bio: Shelly Garg, Attorney, is a Partner with Amin Talati Wasserman and practices in the areas of food, beverage, dietary supplements, cosmetics, medical devices, over-the-counter and homeopathic drugs, and animal and veterinary products. She assists foreign and domestic businesses, manufacturers, distributors, and importers with regulatory compliance and trade and enforcement matters involving FDA, FTC, USDA, EPA, CPSC, TTB, and other federal, state, and local authorities. Noted for her creative leadership, she provides counsel to clients in areas such as strategic business planning, product development, testing and approval, advertisement and promotion, liability risk, inspections, import detentions, import alerts, and related issues. Her keen insights into the FDA and its inner workings have proved to be of significant value to her clients in successfully resolving matters before the agency.

Computer Requirements:

Please read the Webinar Terms and Conditions before you register.

Webinar Details

Date & Time

June 24, 2020

1:00 PM EDT

Length

1 hour 30 minutes
Comprised of 1 hour of commentary and 30 minute Q&A session

Instructor

Cost

1 Participant: $195.00
2-5 Participants: $146.25 each
(25% discount for all participants)
6 or more Participants: $97.50 each
(50% discount for all participants)

ECoP® EAR or ITAR Renewal Credits

1

Event #: Pending