new-usda’s-national-bioengineered-food-disclosure-standard-update

New USDA’s National Bioengineered Food Disclosure Standard Update

Live Webinar

  • 60 minutes


The presentation will help attendees understand the requirements of the National Bioengineered Food Disclosure Final Rule and the New Rule on Hemp Production.


1.  Ingredients subject to Disclosure
2.  Acceptable Labeling Methods of Disclosure
3.  GMO Disclosure symbols that may be Used.
4.  Thresholds for bioengineered foods and exemptions
5.  Timelines for Implementation of the Final Rule.
6.  New Rule on Hemp Production
7.  Instructions for Validating Refining Process for Bioengineered Food Disclosure


Join this session with our expert Norma Skolnik, Where You will find out how it will impact your product labeling and marketing and how to comply to avoid regulatory trouble.

Session Highlights:

  • To understand how the National Bioengineered Food Disclosure Law will impact food labeling in the U.S.

  • To learn how GMO foods must be properly labeled to comply with this new regulation.

  • To learn about the new rule on Hemp Production

  • To update knowledge of new requirements for GMO labeling and validating the refining process for bioengineered foods.

Why You Should Attend:

The USDA recently unveiled its long-awaited BIOENGINEERED FOOD  DISCLOSURE FINAL RULE, the National Bioengineered Food Disclosure Standard, which provides food companies with guidance about how to label products made with genetically modified ingredients. This important Final rule implements the National Bioengineered Food Disclosure Law of 2016 and will impact most food companies and their products.  You should attend to find out how it will impact your product labeling and marketing and how to comply to avoid regulatory trouble.

Who Should Attend:

  • Regulatory managers and regulatory associates, Marketing managers, Product managers in the Food industry

  • Food product manufacturers, distributors, and packers.

  • Anyone involved with Food product labeling and marketing


*You may ask your Question directly to our expert during the Q&A session.

** You can buy On-Demand and view it as per your convenience.

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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