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Health Canada Regulations on NHP's vs. FDA's Dietary Supplement Regulations - Webinar

  • ID: 4899672
  • Webinar
  • May 2019
  • Region: Canada
  • 180 Minutes
  • Compliance Online
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Why Should You Attend:

Attend this webinar to learn overview of what Health Canada considers to be a Natural Health product and review Canadian regulations for Natural Health Products. It will compare Canadian requirements with U.S. FDA requirements for marketing dietary supplements and convey an understanding of how they differ.

References to all relevant Health Canada NHP regulations, FDA regulations, Guidance documents and FDA websites will be provided along with regulatory know-how tips

Areas Covered in the Webinar:

How Natural Health Products are Defined by Health Canada
Product Licensing requirements and Health Canada approval process
NHP Site License requirements
NHP Submission requirements
Advertising Guidelines for NHPs
U.S. FDA Dietary Supplement Regulatory Requirements
How U.S. Dietary Supplement Regulations differ from Canada’s
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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.
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