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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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January 20, 2015 |
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CfPA-The Center for Professional Advancement, New Brunswick, NJ
October 14-16, 2015
Who Should Attend?
This course is intended for all those involved in the regulatory aspects of cosmetics, OTC drugs and personal care products especially:
• Marketing Personnel
• Export and sales 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.
RAPS - Regulatory Affairs Professional Society
This course has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's recertification of their Regulatory Affairs Certification (RAC) upon full completion. 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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| Debra Redbourn; Cosmetic Regulations Advisor, dR Cosmetic Regulations, UK |
Debra Redbourn has been a consultant since 1996 advising companies on the regulations affecting the marketing of cosmetic products in the EU and internationally.
She is a graduate in Cosmetic Science and Chemistry and was previously Scientific Officer at the UK cosmetic trade association, CTPA. Ms. Redbourn is the author of the Cosmetic Legislation module for the Society of Cosmetic Science (SCS). She has been a regular presenter at conferences, including the Summit Events Sun Protection and Anti-Ageing conferences in London and Singapore and Regulatory Summit in Brussels.
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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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sberg@cfpa.com
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It will review the regulatory bodies, enforcement tools and the relevant legislation and guidance to ensure regulatory compliance.
A detailed review of the EU Cosmetics Regulation explaining the ‘Responsible Person’, Product Information File, including a brief outline of the safety assessment (the Cosmetic Product Safety Report – CPSR), reporting of serious undesirable effects, and notification requirements on the EU Commission’s Cosmetic Product Notification Portal (CPNP).
Cover claims from the perspective of affecting the product classification and acceptability to the various regulatory and self-regulatory bodies, with plenty of examples to demonstrate the restrictions and risks will be presented.