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US Cosmetic Manufacturing Regulation - FDA CFR Title 21

 
  January 17, 2018  
     
 
The Center for Professional Innovation & Education, Los Angeles, CA USA
February 28 - March 2, 2018


US Cosmetic Regulation & Manufacturing Training Course

Course Description - Course runs 9:00 - 5:00 on Day 1 & Day 2 -- 9:00 - 3:00 on Day 3 (Breakfast & Lunch Included)

 

This US Cosmetic Regulation & Manufacturing course provides an in-depth guide to the US cosmetic legislative framework. Key focus is placed on helping the participants to successfully navigate both existing US cosmetic regulations and anticipated future legislation. A brief overview of international regulations will be given to help the participants develop global perspectives. Workshops with actual case studies will be conducted throughout the course to bring the participants closer to the reality of marketing cosmetic products in the US.Why This Course Matters

Cosmetic products marketed in the US are regulated under the authority of the Food & Drug Administration (FDA). The regulations pertinent to cosmetic products are published in Title 21, Code of Federal Regulations, in particular, parts 700 to 740. In addition, new legislation such as the Safe Cosmetics Act of 2011 is emerging and may lead to more stringent requirements in the foreseeable cosmetic manufacturing future. Today's consumer cosmetic companies face a tremendous task of bringing newer, better products into the market within a much shorter time frame. A successful market entry strategy often incorporates complex configuration of consumer trend analysis, scientific know-how, efficiency in product development and supply chain management. It is also essential to factor in regulatory feasibility analysis early in the game to avoid unexpected, last minute delay in product launch.

Who Should Attend

This three-day course is designed for professionals in the personal care, cosmetic and pharmaceutical industries engaged in all phases of cosmetic product development, including:

›           Research & Development

›           Technology, Formulation & Product Development

›           Marketing & Technical Sales

›           Regulatory Affairs

›           QA & QC Professionals

›           Business Decision Makers

 
 
Organized by: Center for Professional Innovation & Education
Invited Speakers:

Wen Schroeder

Wen Schroeder

Specialties: Skin/Cosmetics

Wen Schroeder is the founder and president of SEKI Cosmeticals. With 20+ years of industrial experience, 30 US patents and author of numerous publications, Ms. Schroeder is an internationally recognized lecturer on cosmetic science & regulatory affairs.

Her lecture topics cover a wide range of areas including chemical management and biocide regulations, food, drug and cosmetic law. She is a key expert for numerous cross-governmental aid programs including the ASEAN-EU Programme, under the European Commission, for Regional Integration Support in cosmetic & pharmaceutical GMP and testing. Ms. Schroeder is scientific advisor to Taiwan External Trade Development Council and previously taught courses addressing cosmetics, food, OTC drugs, biocides and chemical management topics. She served on the Personal Care Products Council and is active in the Society of Cosmetic Chemists and the Regulatory Affairs Professional Society.

Ms. Schroeder is the editor of a newly published book, Sustainable Cosmetic Product Development by Allured Books, which is the first comprehensive technical reference work in this field for the cosmetic and personal care industry.

 
Deadline for Abstracts: N/A
 
Registration: https://www.cfpie.com/ProductDetails.aspx?ProductID=220
E-mail: info@cfpie.com
 
   
 
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