Labelling of gmo s in the usa
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Labelling of GMO’s in the USA PowerPoint PPT Presentation


This event will offer an overview of the status of GMO’s/Genetically Engineered foods in the USA, how they are regulated by the FDA, FDA’s Biotechnology Policy and Consultation program, and GMO labeling regulations around the world. U.S. State, federal and consumer initiatives to require GMO food labeling in the USA will be discussed, including the soon to be enacted Vermont GMO Labeling law 120. Useful regulatory references will also be provided.Please provide key Learning Objectives of your Topic –a. To learn about the regulatory status of GMOs in the USA; b. To review worldwide GMO Labeling rules; c. To cover FDA’s Biotechnology policy; d. to review FDA’s Biotechnology Consultation program; e. to understand Vermont’s labeling law and the status of other state GMO Labeling proposals. f. To understand what’s happened re: federal GMO labeling legislation. g. to understand industry reaction to the GMO labeling issue.

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Labelling of GMO’s in the USA

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Labelling of gmo s in the usa

Labelling of GMOs in the USA

Speaker: NORMA SKOLNIK| Date: 17th May 2016 2016 2016 | 10:00 AM PST | 01:00 PM EST

Contact Us : Email: support@grcts.com | Tel: +1-248-233-2049


Description

This event will offer an overview of the status of GMOs/Genetically Engineered foods in the USA, how they are regulated by the FDA, FDAs Biotechnology Policy and Consultation program, and GMO labeling regulations around the world. U.S. State, federal and consumer initiatives to require GMO food labeling in the USA will be discussed, including the soon to be enacted Vermont GMO Labeling law 120. Useful regulatory references will also be provided.

Please provide key Learning Objectives of your Topic a. To learn about the regulatory status of GMOs in the USA; b. To review worldwide GMO Labeling rules; c. To cover FDAs Biotechnology policy; d. to review FDAs Biotechnology Consultation program; e. to understand Vermonts labeling law and the status of other state GMO Labeling proposals. f. To understand whats happened re: federal GMO labeling legislation. g. to understand industry reaction to the GMO labeling issue.

Description:


Areas covered in the session

  • Safety of GMOs

  • Regulatory status of GMOs in the USA

  • Worldwide GMO labeling regulations

  • FDA s Position on GMOs

  • FDA Biotechnology Policy

  • FDA Biotechnology Consultation Program

  • State and Consumer initiatives re: GMO Labeling

  • Vermont Labeling law

Areas Covered in the Session:


Who will benefit

  • R&D

  • Manufacturing Engineering

  • Design Assurance

  • Quality Assurance

  • Operations

  • Document Control

Who will benefit:


Instructor profile

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 as Associate Director of Marketed Product Support for Lederle Laboratories and Associate Director of Regulatory Affairs for Wyeth. She currently works as a regulatory consultant.

Instructor Profile :


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