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CfPA-The Center for Professional Advancement, Amsterdam, The Netherlands
23-24 April 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, Director, North America Regulatory Affairs, Colgate-Palmolive Company |
Jennifer R. Martin is currently Director of North America Regulatory Affairs for the Colgate-Palmolive Company. In her current role, she determines strategy and regulatory pathways for Colgate’s complete portfolio of personal care, home care and oral care businesses. Prior to joining Colgate, Jennifer was Global Director of Regulatory, Toxicology and Government Affairs for Edgewell Personal Care, LLC, a standalone company spun off from Energizer Holdings. Before joining Energizer, Ms. Martin was Director of Regulatory, Product Safety and Formula Control for Limited Brands and she also worked in Scientific Regulatory Affairs for the Gillette Company. She began her career at the Cosmetic, Toiletry and Fragrance Association (CTFA, now known as the Personal Care Products Council or PCPC), where her most recent position was Director of International Technical and Regulatory Affairs. Ms. Martin received her Master’s Degree in International Affairs from American University and her undergraduate degree in History and Spanish from the Maryland university system.
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.