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Regulatory Compliance for Food Supplements in the EU - Registration, Labeling, Acceptable Marketing Claims

in IFSQN Events Calendar
Added by COCOM , 30 Apr 2014


Taking place 08 May 2014 (Single Day Event)

COCOM


Logo URL
Event Organizer ComplianceOnline
Contact Name Referral
Contact Number +1-650-620-3915
Contact Email referral@complianceonline.com
Event Category Conference, Live Webinar
Event State/City Palo Alto
Event Country United States
Cost of Attendance $299
Event/Registration URL http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702545?channel=IFSQN

Event Description


This 90-minute webinar will discuss regulatory requirements for food supplements in the EU. It will cover regulatory structure, registration, labeling, supplement ingredient criteria/safety and advertising considerations. Borderline products such as medicinal and herbal products will also be discussed.

Why Should You Attend:
A growing public demand for Food Supplements has resulted in a flurry of companies creating and marketing supplements in the EU. With 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.
This 90 minute webinar on food supplements will review the directives, regulations and authoritative bodies that impact Food Supplements in the EU and will discuss how to verify that products are compliant with published regulations. Validity of Food Supplement ingredients will be discussed along with novel foods, medicinal foods and other borderline products. We will cover detailed requirements for registration, labeling and acceptable marketing claims and touch on subtle differences within EU member states.

Who Will Benefit:
-Nutraceuticals, dietary supplement manufacturers, pharmaceutical companies, food manufacturers and food supplement ingredient suppliers (including chemical and flavor manufacturers) will benefit from this training.
-Executives/Managers within Dietary/Food Supplement companies
-Regulatory Compliance Professionals in the Supplements area
-Quality Assurance or Quality Control Professionals
-Dietary/Food Supplement Manufacturers & Distributors
-Sales/Marketing Personnel in the Supplement Industry

Instructor Profile:
James Russell, is the Director of Business Development and Regulatory Affairs for RJR Consulting Inc, a leading global regulatory consulting firm servicing the Life Science and Consumer Products industries. Mr. Russell has 14 years of experience in the Life Science field, encompassing foods, dietary supplements, pharmaceuticals and medical devices.
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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