Description
FDA is the federal agency that is responsible for overseeing most of the U.S. food supply, medical devices, drugs, cosmetics, vaccines, and tobacco products. FDA is responsible for protecting the public health by ensuring the safety and security of these products.
Recent changes in the broader regulatory environment and advancements in technology are shifting the way the FDA operates.
In this webinar, presenters discuss:
- The New Policy, Legal, and Regulatory Landscape
- FDA & Artificial Intelligence: Promise and Prospect
- FDA’s Human Foods Program
- What Importers Need to do Now in the New FDA Environment
Presenters:
- Jennifer Diaz, President, Diaz Trade Law
- Rick Quinn, Of Counsel, Diaz Trade Law
Who should attend?
- Importers
- Manufacturers
- Customs Brokers
- Regulatory Affairs Professionals
- In-house Legal Counsel
- Product Development Managers
- Others interested in FDA
Shane –
It was a well thought out presentation covering all the changes in FDA.
Jon –
This was a very informative webinar on the practical implications of the new FDA Nationalized Entry Review.
Jessica –
Great overview!!!!!!
Bonnie –
Well organized with a broad scope of information addressing FDA regulated importations.
Frank –
Jen always provides a great perspective on the topic at hand and really breaks it down into the important points!