FDA Regulation of Dietary Supplements in the USA

Event Information
Product Format
Prerecorded Event
Presenter(s)
Conference Date
Tue, Mar 21, 2017
Length
60 minutes
Product Description

Understanding the Essential Regulations for Marketing and Labeling Dietary Supplements

 

In order to market dietary supplements successfully in the USA and to avoid regulatory problems, it’s essential to understand US FDA dietary supplement regulations.

This webinar with expert speaker Norma Skolnik will cover essential and significant regulations for the marketing and labeling of US dietary supplements. It will also cover permissible dietary supplement claims and ways to avoid regulatory challenges that could get a company in trouble. References to all FDA regulations and policies regarding Dietary Supplements will be provided as well as know-how tips for marketing dietary supplements without regulatory issues.

Session Highlights:

  • FDA Regulations for Marketing Dietary Supplements in the USA
  • Dietary Supplement Claims
  • Marketing New Dietary Ingredients
  • Dietary Supplement Labeling and Advertising Rules
  • Dietary Supplements GMPs
  • FDA Enforcement and Dietary Supplement Warning letters

Who should attend?

  • Regulatory Affairs Managers, Directors & Associates
  • Product Safety Managers
  • Compliance Specialists
  • Marketing managers
  • Personnel involved in planning to market or label dietary supplement products in the U.S.A.

Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.

Order Below or Call 1-866-458-2965 Today

Order Form

(Select the format below)



You can also order through:

1-866-458-2965

1-800-508-2592

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
More Events By The Speaker

Why AudioEducator?
  • Save money on travel.
  • Meet your specific training needs.
  • Keep learning after the event.
  • Save time training your whole staff.