Dietary Supplements - Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates

Instructor: James Russell 
Product ID: 702154
  • Duration: 90 Min
This training will review the dietary supplement regulations in the USA and explain how to verify that your products are compliant with the most recent regulations and provisions. It covers the FDA regulatory structure and considerations for manufacturing, labeling and advertising dietary supplements.

recorded version

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: Jul-2016

Training CD / USB Drive

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: [email protected]

Read Frequently Asked Questions

Why Should You Attend:

With the FDA beginning to take a stronger stance on Dietary Supplement enforcement, it is important for companies to verify that their products comply with the latest regulations and provisions.

This 90 minute training will review the dietary supplement regulations and discuss how to verify that your products are compliant, while citing differences with food and drug regulations. We will also cover what qualifies a material as a dietary ingredient, considerations for manufacturers and distributors, requirements for compliant labeling and acceptable marketing claims. An update on FDA’s draft guidance for New Dietary Ingredients and an overview of the Dietary Supplement Labeling Act (both introduced in 2011) will also be discussed.

At the conclusion of this 75 minute presentation, there will be a 15 minute Q&A session with the speaker.

Areas Covered in the Webinar:

  • Dietary Supplement Overview
    • What is a dietary supplement?
    • Supplements vs. Pharmaceuticals/OTC Drugs/Conventional Foods.
  • Regulatory Structure
    • FDA Structure regarding Dietary Supplements.
    • Industry Groups.
  • History of Dietary Supplement Regulation
    • Early History & DSHE.
    • Code of Federal Regulations.
  • Manufacturing/Distributor Considerations
    • Company & Facility Registration.
    • GMP Requirements.
  • 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 Requirements.
    • Labeling Claims.
    • Health vs. Disease vs. 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.
    • Disclosures & Claim Substantiation.
    • Testimonials.
  • Current Events
  • Questions & Answers.

Who Will Benefit:

This course will be beneficial to the following personnel in Dietary Supplement manufacturing companies:

  • Executives of Dietary Supplement companies
  • Regulatory Compliance Professionals
  • Quality Assurance Professionals
  • Dietary Supplement Manufacturers
  • Dietary Supplement Distributors
  • Sales/Marketing Personnel

Instructor Profile:

Mr. Russell, is the Director of Regulatory Affairs and Business Development for RJR Consulting Inc, a leading global regulatory consulting company servicing the Life Science and Consumer Products industries. Mr. Russell has 14 years of experience in the Life Science field, encompassing foods, dietary supplements, medical devices and pharmaceuticals. James joined RJR Consulting in 2009 to assist companies with their global regulatory, manufacturing and distribution needs. Prior to RJR, Mr. Russell worked for a large life science distribution company with organizational responsibilities including supply chain, regulatory, device business strategy and product data quality. Mr. Russell is also a participating member of the Regulatory Affairs Professionals Society (RAPS) and associate member of the Consumer Healthcare Products Association (CHPA).

Follow us :
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices

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 [email protected] call +1-888-717-2436 (Toll Free).

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