Regulation of Natural Health Products in Canada

Event Information
Product Format
Prerecorded Event
60 minutes
Product Description

Health Canada’s Regulations on Natural Health Products vs. FDA’s Dietary Supplement Regulations

In this session with expert speaker Norma Skolnik, you’ll get an overview of what is considered a Natural Health product by Health Canada and review Canadian regulations as they apply to Natural Health Products. Get pertinent information on marketing dietary supplements through a comparison of Canadian requirements with that of the U.S. FDA to develop an understanding of the significant differences between the two.

Plus, get references to all relevant regulations, both Health Canada NHP regulations and FDA regulations, as well as references to guidance documents and websites. You will come away from this session with useful regulatory knowledge and know-how for compliance

Session Highlights:

  • Canadian Regulatory Structure
  • How Natural Health Products (NHPs) are Defined by Health Canada
  • Product Licensing requirements and Health Canada approval process
  • NHP Site License requirements
  • NHP Submission requirements
  • NHP Monographs
  • Manufacturing/Quality Requirements for Natural Health Products
  • Canadian NHP Labeling & Advertising Guidelines for NHPs
  • U.S. FDA Dietary Supplement Regulatory Requirements
  • How U.S. Dietary Supplement Regulations differ from Canada’s NHP requirements

Who should attend?

  • Regulatory Affairs managers, directors & associates
  • Product Safety managers
  • Compliance Specialists
  • Marketing managers and
  • Anyone involved in planning to market or label dietary supplements/ Natural Health Products in Canada and/or the U.S.A.

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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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