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CfPA-The Center for Professional Advancement, New Brunswick, NJ
October 18-19, 2018
Who Should Attend?
This course is intended for all those involved in the regulatory aspects of cosmetics, OTC drugs and personal care products especially:
• Regulatory Affairs Practitioners, including Attorneys and Paralegals
• Corporate compliance officers
• Marketing Personnel
• Research and Product Development Personnel
• QC and QA Professionals
• Cosmetic Chemists
Operational, legal and management professionals who are commencing their careers in regulatory affairs or product compliance will likewise find this course extremely valuable. Course Description
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Organized by:
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CfPA-The Center for Professional Advancement |
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Invited Speakers:
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| Jennifer R. Martin; Global Director of Regulatory, Toxicology and Government Affairs, Edgewell Personal Care, LLC |
Jennifer R. Martin is currently Global Director of Regulatory, Toxicology and Government Affairs for Edgewell Personal Care, LLC, a standalone company spun off from Energizer Holdings in July 2015. In her current role, she defines global compliance and product safety policy, position and strategy and represents Edgewell to governments and trade organizations around the world. For ten years prior to joining Energizer, Ms. Martin was Director of Regulatory, Product Safety and Formula Control for Limited Brands. She spent fifteen years with the Cosmetic, Toiletry and Fragrance Association (CTFA, now known as the Personal Care Products Council or PCPC) in Washington, D.C., most recently as Director of International Technical and Regulatory Affairs. Ms. Martin lives in Connecticut with her three beloved children who make it all worthwhile. Ms. Martin received her Master’s Degree in International Affairs from American University.
Additional Faculty
Sandra Browne, Sr. Manager, International Regulatory Affairs, Wilkinson Sword GmbH
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Deadline for Abstracts:
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n/a
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Registration:
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Please click here for registration information.
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E-mail:
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jmorbit@cfpa.com
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It will review the regulatory bodies, enforcement tools and the relevant legislation and guidance to inform regulatory compliance. This will include key agencies having jurisdiction over cosmetics, with emphasis on the U.S. FDA, the European Commission and the state of California, among others.
There will be a detailed discussion of ingredient restrictions based on their function in the finished formulation. In addition to a full review of labeling requirements, we will consider how claims impact a product’s regulatory classification and its acceptability to the regulator, with examples to demonstrate the restrictions, risks and current enforcement priorities.