GMPs and Adulteration - Understanding FDA Regulation of Cosmetics
This webinar will cover key definitions like cosmetic, drug, medical device and adulteration including core concepts like poisonous and deleterious and added vs. non-added adulterants. Attendees will learn how to implement, monitor and verify GMPs for cosmetics. Why Should You Attend: Cosmetics are a unique area of regulation. Good Manufacturing Practices (GMPs or cGMPs) play a crucial role in protecting the consumer and the brand. Despite occupying this pivotal role, confusion pervades about what GMPs to follow, how to implement, monitor and verify GMPs for cosmetic and OTC products. The answer requires looking at key definitions like “adulteration” and understanding core concepts, such as “poisonous and deleterious” and added vs. non-added adulterants. GMPs are more than keeping a tidy facility; they are the crucial vanguard of ensuring a product is safe and avoiding enforcement actions. This webinar will start with the basic regulations to build an understanding of why GMPs are important. It will provide a new perspective and awareness of how to adopt, monitor, verify and change cosmetic GMPs. Areas Covered in the Webinar: Key Definitions
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Cosmetic, Drug, Medical Device Adulteration Poisonous and Deleterious Standard Added vs Non-Added Standards
General Overview of GMPs
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Which GMPs apply to cosmetics? How do they address adulteration?
GMPs and Added Substances
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Foreign contaminants Pesticides New ingredients
GMPs and Labeling
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What is misbranding? Which GMPs address labeling?
GMPs and Sanitation and Aesthetic Adulteration
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GMPs to address operations Common GMP mistakes
Who Will Benefit:
Cosmetic/OTC Industry Executives Cosmetic/OTC Manufacturers/Distributors Medical Device Manufacturers/Distributors In-House Legal Counsel Regulatory Affairs Government Affairs Distributors and MANUFACTURERs Customs Brokers FDA/Food & Drug Attorneys
For more details please visit us at: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=703478/~GMPs_an d_Adulteration__Understanding_FDA_Regulation