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      2-day Interactive Seminar on Regulatory Compliance for Dietary Supplements: Focus on US, EU and Canada - June 13-14, 2022

      Research_and_Markets_Logo

      News provided by

      Research and Markets

      May 25, 2022, 06:00 ET

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      DUBLIN, May 25, 2022 /PRNewswire/ -- The "Regulatory Compliance for Dietary Supplements in the US, EU and Canada" training has been added to ResearchAndMarkets.com's offering.

      This 2-day interactive virtual seminar will review the regulations that impact Dietary Supplements in the US, EU, and Canada and discuss how to verify that products are compliant with these regulations. Differences with food and drug regulation in these countries will be noted as well.

      A growing public demand for supplements has resulted in a flurry of companies creating and marketing dietary supplements in the United States, EU, and Canada.

      With the regulatory authorities beginning to take a stronger stance on enforcement of regulatory policies, procedures and GMP compliance, it is important for companies to verify that their products comply with the latest regulations and provisions if they plan to market Supplements in these countries.

      We will also cover what qualifies as a dietary supplement or dietary ingredient, how to ensure GMP compliance as well as detailed requirements for labeling and acceptable marketing claims. An update on current events within the Supplement industry and the potential impacts to Manufacturers and Distributors in the US, EU, and Canada will also be presented and discussed.

      Key Topics Covered:

      DAY 01 (9:00 AM - 5:00 PM EDT)

      Session Start Time: 9:00 AM


      Dietary Supplement Regulation in the U.S.

      • Dietary Supplement Overview
      • What is a dietary supplement?
        • Supplements vs.
        • Pharmaceuticals
        • OTC Drugs
        • Conventional Foods
        • Medical foods
        • Natural products
        • Herbal medicinal products

      Organizations and Regulatory Structure

      • FDA Structure regarding Dietary Supplements
      • Industry Groups

      History of Dietary Supplement Regulation

      • Early History
      • DSHEA
      • Code of Federal Regulations

      Manufacturing Considerations

      • Company & Facility Registration
      • GMP Requirements
      • GMP inspections

      Dietary Ingredients

      • What qualifies as a dietary ingredient?
      • Old dietary ingredients vs. New dietary ingredients
      • New Dietary Ingredient Notification (NDIN)
      • Updated New Dietary Ingredient Guidance from FDA

      Labeling Considerations

      • Display Panels & Layout
      • Supplement Facts Panel
      • Labeling Claims
        • Health claims
        • Disease Claims
        • Structure/Function claims
        • Disclaimers/Substantiation
      • Notification of labeling claims to FDA
      • Dietary Supplement Labeling Act

      Advertising Considerations

      • FDA vs. FTC jurisdiction
      • Enforcement
      • Expressed vs. Implied Claims
        • Exercises & examples
      • Disclosures
      • Claim Substantiation
      • Testimonials

      DAY 02 (9:00 AM - 5:00 PM EDT)

      Food Supplement regulation in the EU


      Overview

      • What is a food supplement?
      • Borderline products
      • Medicinal Foods

      Organizations and Regulatory Structure

      • EU Regulatory Structure
      • Industry Groups

      Supplement Regulation

      • Early History
      • Food Supplement Directive

      Manufacturing Considerations

      • Company & Facility Registration
      • GMP Requirements

      Dietary Ingredients

      • What qualifies as a dietary ingredient?
      • Ingredient safety
      • RDA vs RDI
      • DRV vs % Daily Value

      Labeling Considerations

      • Display Panels & Layout
      • Labeling Claims
        • Health claims
        • Disease Claims
        • Reduction of Disease Risk Claims
        • Nutrition Claims
      • Notification requirements

      Advertising Considerations

      • Enforcement
      • Claim Substantiation

      Natural Health Product Regulation in Canada

      Overview

      • What is a Natural Health Product?

      Organizations and Regulatory Structure

      • Canadian Regulatory Structure
        • Health Canada
        • Canadian Health Products Directorate

      Supplement Regulation

      • National Health Products Regulation
      • Differences between Canada and US
      • Supplements monographs
      • Requirements for pre-market approval

      Manufacturing Requirements for Natural Health Products in Canada

      Dietary Ingredients


      Labeling Considerations


      Advertising Considerations


      Enforcement and Post-Marketing Surveillance

      • Review of Current Events and other Industry Topics Questions and Answers

      For more information about this training visit https://www.researchandmarkets.com/r/dgr8g6

      Media Contact:

      Research and Markets
      Laura Wood, Senior Manager
      [email protected]

      For E.S.T Office Hours Call +1-917-300-0470
      For U.S./CAN Toll Free Call +1-800-526-8630
      For GMT Office Hours Call +353-1-416-8900

      U.S. Fax: 646-607-1907
      Fax (outside U.S.): +353-1-481-1716

      SOURCE Research and Markets

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