ComplianceOnline

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

Instructor: Norma Skolnik
Product ID: 705497
  • Duration: 60 Min

recorded version

$279.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Nov-2017

Training CD / USB Drive

$379.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This online training will offer an overview of what Health Canada considers to be a Natural Health product (NHP) and review Canadian regulatory requirements for Natural Health products. It will compare Canadian requirements with U.S. FDA requirements for marketing and labeling dietary supplements and convey an understanding of how they differ.

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

Who Will Benefit:

  • Regulatory Affairs managers
  • Directors & Associates
  • Product Safety managers
  • Compliance Specialists
  • Marketing managers
Instructor Profile:
Norma Skolnik

Norma Skolnik
Regulatory Consultant, EAS Consulting Group and NS Consulting

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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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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