FDA Regulations for Cosmetics and New Legislation

Pre Recorded

  • 60 minutes

Cosmetic regulations are changing and FDA is looking at cosmetic marketing more closely than ever. New legislation for Cosmetics was proposed in 2015 and once passed into law, will increase and strengthen regulatory requirements for cosmetics and personal care products. In this informative webinar with expert Norma Skolnik, you will learn about current FDA regulations and requirements for marketing and labeling cosmetics and about the new requirements to be implemented once the Personal Care Products Safety Act of 2015 is passed. Helpful insights and know-how tips will be provided.

Session Highlights:

  • Learn about laws & regulations applicable to Cosmetics in the U.S. 

  • Review FDA Cosmetic Labeling requirements 

  • Understand cosmetic claims and compliance issues 

  • Gain an understanding of what “Cosmeceuticals” are and how they can be legally marketed 

  • Learn about the 2015 Proposed Cosmetics legislation, the Personal Care Products Safety Act 

  • Understand Adverse Event Labeling & Reporting requirements for cosmetics and how these will change under the Personal Care Products Safety Act.

Why You Should Attend:

This webinar will provide you with what you need to know to market cosmetic and personal care products in compliance with the latest FDA regulations and prepare you for forthcoming cosmetic legislation.

Who Should Attend:

  • Regulatory Managers, Directors, and Associates

  • Compliance managers

  • Product Safety and Technology Managers

  • Cosmetic marketing professionals

  • Those in the Cosmetic or Personal Care Products industries, as well as those in the Consumer Healthcare Industry

Norma Skolnik

Norma Skolnik

Norma Skolnik is currently a Regulatory Consultant with over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She was Director of Regulatory Affairs for the Americas for Cadbury Adams and Director of Regulatory Affairs for the Adams division of Pfizer before that. Prior to that she was Associate Director of Regulatory Affairs for the Warner-Lambert company and Associate Director Regulatory Affairs at American Home Products Whitehall-Robbins Division.

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