Speaker Profile

James E. Russell
Director of Regulatory Affairs, RJR Consulting Inc

Mr. Russell is the Director of Regulatory Affairs and Business Development for RJR Consulting Inc, a leading global regulatory consulting firm servicing the Life Science and Consumer Products industries. Mr. Russell has 13 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 regulatory, supply chain, business strategy and product data quality. Mr. Russell currently teaches on a variety of regulatory topics and is a participating member of the Regulatory Affairs Professionals Society (RAPS).

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Speakers

Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA

This 90 minute live, interactive webinar 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 An update on FDA’s draft guidance for New Dietary Ingredients and an overview of the Dietary Supplement Labeling Act (both introduced in 2011) will also be discussed.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.

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Speakers

3-Hour Virtual Seminar on Regulatory Compliance for Food Supplements in the EU

A growing public demand for Food Supplements has resulted in a flurry of companies creating and marketing supplements in the EU. With the regulatory authorities taking a strong stance on enforcement of regulatory policies and procedures, it is important for companies to verify that their products comply with the latest regulations and provisions if they plan to market Food Supplements in the EU.

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Speakers

Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA

This 90 minute live, interactive webinar 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.

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