usda-gmo-labeling-update

USDA GMO Labeling Update

Pre Recorded

  • 60 minutes

GMO labeling is a controversial topic and there have been many different approaches to GMO labeling, with individual states attempting to have their own labeling laws. Finally, a federal law was passed last year that preempts state laws, but there are still some unresolved issues that will be addressed in this audio conference.

This session by expert speaker Norma Skolnik will discuss how to effectively label products with GMO ingredients and still comply with regulatory requirements. It will also cover what to expect when the July 2018 USDA regulations will be issued. Norma will provide you with references to all relevant FDA regulations, guidance documents, and FDA websites for GMO labeling. You will also gain regulatory insights and will learn about the FDA contacts and know-how tips.


Session Highlights:

  • Status of GMO’s in the USA

  • FDA Position on GMO’s/GE foods

  • FDA Biotechnology Policy & Consultation Program

  • Worldwide GMO Labeling Regulations

  • State Initiatives & Vermont Law re: GMO Labeling

  • July 2016 Compromise GMO Labeling Bill

  • What to Expect from the USDA July 2018 regulations


Why You Should Attend:

This webinar will help you learn about the history and current status of GMO Labeling in the USA. There have been many different approaches to GMO labeling, with individual states attempting to have their own labeling laws. A federal law was passed last year that preempts state laws, but there are still some unresolved issues that will be addressed in this webinar. This presentation will show you how to effectively label products with GMO ingredients and still comply with regulatory requirements. It will also cover what to expect when the July 2018 USDA regulations will be issued.


Who Should Attend:

  • Food marketing managers

  • Regulatory Affairs managers and associates in the Food Industry

  • Labeling managers at Grocery & Food companies

  • Food & Grocery manufacturers and distributors


Ask your question directly from our expert during the Q&A session following the live event.

Norma Skolnik

Norma Skolnik

Norma Skolnik is currently a Regulatory Consultant with over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She was Director of Regulatory Affairs for the Americas for Cadbury Adams and Director of Regulatory Affairs for the Adams division of Pfizer before that. Prior to that she was Associate Director of Regulatory Affairs for the Warner-Lambert company and Associate Director Regulatory Affairs at American Home Products Whitehall-Robbins Division.

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