How to Prepare For the DARK Act/ GMO Labeling Webinar by Norma Skolnik

Impact of New GMO Labeling Bills & How to be Prepared

Event Information
Product Format
Prerecorded Event
Presenter(s)
Length
60 minutes
Product Description

Impact of the DARK Act/ GMO Labeling Standards and How to Stay Prepared


Congress introduced a compromise bill that would create a mandatory, national labeling standard for GMO foods. Although this bill is the first mandatory legislation introduced in Congress it falls short of what consumers expect — a simple at-a-glance disclosure on the package. As written, this compromise might not even apply to ingredients derived from GMO soybeans and GMO sugar beets.

Join expert speaker Norma Skolnik in this Live Webinar which offers an overview of the status of GMO’s in the U.S.; how they are regulated by the FDA and attempts like the Safe & Accurate Food Labeling Act of 2015, also known as the “DARK Act” to legislate their labeling. Norma will also review state initiatives to require GMO labeling in the USA, which prompted the “DARK Act”.

Session Highlights:

  • Safety of GMOs
  • Regulatory status of GMO’s in the USA
  • FDA’s Biotechnology Policy & Consultation Program
  • Current state initiatives re: GMO Labeling
  • The Safe & Accurate Food Labeling Act, also called the “DARK Act”
  • Other recent legislative attempts re: GMO Labeling

Who Should Attend

  • Regulatory Affairs managers
  • Directors & associates
  • Product Safety managers
  • Compliance Specialists
  • Food labeling managers
  • Marketing managers
  • Anyone involved in planning to market or label GMO food products in the U.S.A.

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1-866-458-2965

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1-919-287-2643

About Our Speaker

Norma Skolnik - FDA Regulations Expert

Norma Skolnik has over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She served as Director of Regulatory Affairs for the Americas for Cadbury Adams. Prior to that, she was Director of Regulatory Affairs for the Adams Division of Pfizer and Associate Director of Regulatory Affairs for the Warner-Lambert company. She also served as Director of Regulatory Affairs for Lederle Consumer Healthcare and...   More Info
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