2 Day In Person Seminar On Regulatory Compliance For Dietary Supplements The Us Eu And Canada - USA

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 - The venue will be

announced soon.

Participants of this RAPS-approved seminar can earn 12

RAC points.

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.

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

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 monitoring

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).

DATE AND VENUE:

September 13 and 14, 2012

Seminar Timings: 8am to 5pm EDT

Place: Boston

Venue: To Be Announced

Price –$ 1695; Register for 4 Participants to Get 1 Free Pass.

Discounts offered for multiple registrations.

Please contact Customer Care at 1800 447 9407

Contact Information:

Event Coordinator

Toll free: 1800 447 9407

Fax: 302 288 6884

Email: support@globalcompliancep anel.

com

Website: https: www.

globalcompliancepanel.

com/

GlobalCompliancePanel

NetZealous

1000 N West Street,

Suite 1200, Wilmington,

DE 19801 - USA

Company Contact:

• Posted By: GlobalCompliancePanel

• Phone: 8004479407

• Address: 1000 N West Street, Wilmington , DE , USA

• Email:

• Website: http://www.globalcompliancepanel.com

• Business Description: GlobalCompliancePanel is an online training gateway delivering high quality regulatory & compliance trainings in a simple, cost effective and in a user friendly format.
  
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