ComplianceOnline

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.

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. 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.

Who will Benefit

  • Executives/Managers within Dietary Supplement or Natural Product companies
  • Regulatory Compliance Professionals in the Supplements or Natural Products area
  • Quality Assurance or Quality Control Professionals
  • Dietary Supplement or Natural Product Manufacturers & Distributors
  • Sales/Marketing Personnel in the Supplement or Natural Product Industries

In-Person Seminar going Virtual with increased learner satisfaction.

Yes, attend this seminar from anywhere. We are making it real and more interactive – Here's a sneak peek:

Our enhanced delivery process and technology provides you an immersive experience and will allow you to access:

  • The real-time and live presentation as in in-person events
  • Private chat for company-specific conversation – the same as you would get in an in-person seminar
  • Opportunities to connect with your peers to share knowledge at a different time and have group discussions
  • Live workshop activities
  • Live Q&A during the event and offline Q&A assistance after the event
  • Certification
Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure
Day 01(8:00 AM - 4:00 PM EDT)
  • Session Start Time: 8:00 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(8:00 AM - 4:30 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

Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure
Travis Austin MacKay

Travis Austin MacKay
Director of Regulatory Affairs, Plexus Worldwide

Travis MacKay is the Director of Regulatory Affairs for Plexus Worldwide, a leading direct sales company with a range of products dedicated to helping others obtain health and happiness. He currently oversees international regulatory compliance activities driving strategic direction focused on claims development and substantiation strategy, product development and commercialization, international formulation considerations, and quality testing & validation.

Travis has 20 years of quality and regulatory experience, including prior regulatory affairs leadership positions within well-respected, global consumer product companies. He has a passion for mentoring regulatory professionals to develop robust compliance systems that keep business moving forward.

Travis Graduated from the University of Utah in 2002 with a B.S. in Behavioral Science and Health (Human Health Emphasis). He is a fly-fishing enthusiast, a college football fan, an exercise junky, and a lover of classic cars. He escapes the noise by spending time with his family in the outdoors of beautiful Arizona.

Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure

Register Now

Online using Credit card

$1,699.00

(One Dial-in One Attendee)

August 19-20, 2020, Virtual Seminar
(Registrations till July 24, 2020 - $1699)
(Registrations after July 24, 2020 - $2099)

$8,665.00

Group-Max. 10 Attendees

August 19-20, 2020, Virtual Seminar
(Registrations till July 24, 2020 - $8665)
(Registrations after July 24, 2020 - $10195)



Other Registration Option

By order form / PO#

Payment Mode

By Check -
Pay your check to (payee name) “MetricStream Inc” our parent company and Mail the check to:

ComplianceOnline (MetricStream, Inc),
2479 E. Bayshore Road Suite 260
Palo Alto, CA 94303
USA

By Wire -

Register / Pay by Wire Transfer

Please contact us at +1-888-717-2436 to get details of wire transfer option.

Note: In view of Coronavirus situation and travel advisory issued, ComplianceOnline will waive off all cancellation charges for the registrations till June 30, 2020.

Terms & Conditions to Register for the Seminar/Conference/Event

Your registration for the seminar is subject to following terms and conditions. If you need any clarification before registering for this seminar please call us @ +1-888-717-2436 or email us @ customercare@complianceonline.com

Payment:

Payment is required 2 days before the date of the conference. We accept American Express, Visa and MasterCard. Make checks payable to MetricStream Inc. (our parent company).

Cancellations and substitutions for In-person Seminars:

Written cancellations through fax or email (from the person who has registered for this conference) received at least 10 calendar days prior to the start date of the event will receive a refund - less a $300 administration fee. No cancellations will be accepted - nor refunds issued - within 10 calendar days before the start date of the event.

On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($300) will be transferred to any future ComplianceOnline event and a credit note will be issued.

Substitutions may be made at any time. No-shows will be charged the full amount.

We discourage onsite registrations, however if you wish to register onsite, payment to happen through credit card immediately or check to be submitted onsite. Conference material will be given on the spot if it is available after distributing to other attendees. In case it is not available, we will send the material after the conference is over.

In the event ComplianceOnline cancels the seminar, ComplianceOnline is not responsible for any airfare, hotel, other costs or losses incurred by registrants. Some topics and speakers may be subject to change without notice.

Cancellations and Substitutions for Virtual Seminars & Webinars:

Written cancellations through fax or email (from the person who has registered for the training) received at least 10 calendar days prior to the start date of the event will receive a refund — less a 30% administration fee. No cancellations will be accepted — nor refunds issued — within 10 calendar days from the start date of the event. On request by email or fax (before the training) a credit for the amount paid minus administration fees (30%) will be transferred to any future ComplianceOnline event and a credit note will be issued. Substitutions may be made at any time. No-shows will be charged the full amount. Some topics and speakers may be subject to change without notice.
Offers:
  • Early bird seats are limited and based on first-come, first-serve.
  • Multiple offers cannot be combined.
  • Testimonials

    See What People Say About Us

    Presenter was very knowledgeable and able to provide real world examples and address unique concerns of attendees. ComplianceOnline is an excellent resource.

    Regulatory Affairs Manager, LifeVantage

    In-depth look at specific products, claims, disclaimers needed are discussed, but seeing a specific example makes it click in my head. I thought this was very helpful interaction and discussion on topics were very helpful.

    Regulatory Affairs Manager, Basicresearch

    Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure

    We need below information to serve you better

    Best Sellers
    You Recently Viewed
      Loading