Seminar on Regulatory Compliance for Dietary Supplements in the US, EU and Canada
08/17/2012

James E Russell, a senior Regulatory Affairs professional, will host the seminar at Boston on September 13 and 14. Participants of this RAPS-approved seminar can earn 12 RAC points.

Online PR News – 17-August-2012 – San Francisco – Summary:
GlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, “Regulatory Compliance for Dietary Supplements in the US, EU and Canada”. James E Russell, a senior Regulatory Affairs professional, will host the seminar at Boston on September 13 and 14. Participants of this RAPS-approved seminar can earn 12 RAC points.
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Course Agenda:
In the light of exploding demand for supplements in the US, EU and Canada;businesses dealing withthese products are required to meet stringent regulatory policies, procedures and GMP compliance to succeed.
This interactive, live seminar will review these regulations. It will discuss how to verify if products are compliant anddiscuss the differences infood and drug regulations in these countries.
This seminar will cover what qualifies as a dietary supplement or dietary ingredient; how to ensure GMP compliance, and details requirements for labeling and acceptable marketing claims. It will also look at current events in the industry within these markets.
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Course Description:
Day 1 –September 13, 2012
Dietary Supplement Regulation in the U.S
Lecture 1: Dietary Supplement Overview
Lecture 2: Organizations and Regulatory Structure
Lecture 3: History of Dietary Supplement Regulation
Lecture 4:Manufacturing Considerations
Lecture 5: Dietary Ingredients
Lecture 6:Labeling Considerations
Lecture 7:Advertising Considerations
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Day 2 –September 14, 2012
Food Supplement regulation in the EU
Lecture 8: Overview
Lecture 9:Organizations and Regulatory Structure
Lecture 10:Supplement Regulation
Lecture 11:Manufacturing Considerations
Lecture 12:Dietary Ingredients
Lecture 13:Labeling Considerations
Lecture 14:Advertising Considerations

Natural Health Product regulation in Canada
Lecture 15:Overview
Lecture 16:Organizations and Regulatory Structure
Lecture 17:Supplement Regulation
Lecture 18:Manufacturing Requirements for Natural Health Products in Canada
Lecture 19:Dietary Ingredients
Lecture 20:Labeling Considerations
Lecture 21:Advertising Considerations
Lecture 22:Enforcement and Post-Marketing Surveillance
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About the Speaker:
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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DATE AND VENUE:
September 13 and 14, 2012
Seminar Timings: 8am to 5pm EDT
Place: Boston
Venue: Courtyard Boston Logan Airport
225 William F. McClellan Highway, Boston, Massachusetts 02128 USA
Price –$ 1695; Register for 4 Participants to Get 1 Free Pass. Discounts offered for multiple registrations. Please contact Customer Care at 1800 447 9407
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Contact Information:

Event Coordinator
Toll free: 1800 447 9407
Fax: 302 288 6884
Email: support@globalcompliancepanel.com
Website: https://www.globalcompliancepanel.com/
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