International Regulatory Requirements for Dietary Supplements

About this course

Globalization of the economy has provided additional market opportunities while also presenting various challenges. Navigating the various country requirements can be confusing and frustrating. This course provides an overview of the global market statistics and market potential of the nutraceutical and functional food industries. A background and history on the various countries’ legislation and responsible agencies will be provided along with country specific requirements for your company’s products to meet the necessary regulations. Regulatory frameworks for various countries will be discussed providing a comparison of how nutraceutical supplements and functional foods are defined in other countries, along with the differences or similarities between product licensing, providing standards of evidence for a product’s safety and efficacy, site licensing, good manufacturing practices and Adverse Event Reporting. The various countries that will be covered are as follows:

• Brazil
• Germany
• Canada
• Italy
• China
• Spain
• France
• Taiwan
• United Kingdom

Who Should Attend

This course is a must for employees at all levels involved with any activities associated with marketing, international business development, quality control, quality assurance and regulatory compliance roles for companies interested or involved in exporting their dietary supplements or functional food products to
other countries.

Course outline

What You Will Learn

The two-day, “International Regulatory Requirements for Dietary Supplements” course addresses the various regulatory frameworks for selling your product in 9 countries. In addition, participants in this course will also benefit from discussions of other important-to-know topics such as the various country classifications of dietary supplements, relevant safety and efficacy information required for label claims and the individual country’s market potential. This information-packed course is designed with extensive information and resources to ensure your company’s compliance to various country requirements.

Discussion and Working Groups

A significant proportion of the course time will be devoted to group work, where delegates have the opportunity, through case studies, to put theory into practice.

Additionally, discussion periods will provide delegates with plenty of time to obtain answers to their specific questions and concerns.

Venue

Salt Lake City, UT - Marriott City Center

Salt Lake City Marriott City Center
220 South State Street · Salt Lake City, Utah 84111 USA
1-801-961-8700

• Walk to Temple Square, shopping & dining from this AAA 4-diamond Salt Lake City hotel
• Named as one of the best Salt Lake City hotels for quality and service
• Free high-speed Internet access, award-winning service, 15,000 sq ft of event space

Tutors

We believe that our team of experts are the best available. Not only have they got years of experience in the industry, but they are committed to tutoring and helping those inside the industry to improve and raise the standards. We understand that you attend courses to learn about the latest regulations and to get your questions answered.

Our expert for this course is:

• Peter Martin
  MS
  Trading Law Manager

  • [email protected]
  • +1 857 350 4788

What you've said

“NLI is always working to implement the most stringent quality systems and looking for opportunities to prove the superiority of its systems. DSQP certification with NSF-DBA has been another way for NLI to show a commitment to being a CMO of the highest quality. Investment in training ensures your company is in compliance and manufacturing safe products for the public”

Jera’le Smith, Director of Quality Assurance, Nutritional Laboratories International (NLI)

“I attended both NSF-DBA’s FDA inspection Readiness and Corrective Action Management modules and our company assiduously implemented the recommendations made. I am absolutely convinced that doing so was one of the primary reasons our company did not receive an FDA Form 483 following an FDA unannounced 4-day GMP inspection”

Kim Randall Pearson, General Counsel, Thorne Research, Inc.