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  • Cosmetics - How Are they Regulated?

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Wednesday - Mar 12, 2014 10:00 AM
  • End Time:
  • Wednesday - Mar 12, 2014 11:00 AM
  • Location:
  • Online
  • This webinar will provide a comprehensive overview of FDA regulations for cosmetic products. It will help you understand how to be compliant in manufacturing, labeling and advertising of cosmetic products, and thereby ensure successful FDA and state inspections.

    Why Should You Attend:

    This presentation will help the management and staff of cosmetics companies to understand the regulations and how they apply to their products. We will help you gain a strong understanding of what is involved in becoming compliant in manufacturing, labeling and advertising of cosmetic products. Attendees will learn the importance of documenting and following up on consumer complaints, the marketing errors to avoid, the value of tracking lots, maintaining retention samples, having a quarantine area and its purpose, the necessity in using good manufacturing practices (GMP) in the manufacturing of cosmetics and the possibility of needing a quality testing program.

    This session will include the key principles of GMP as defined by FDA as well as incorporate FDA regulatory inspection strategy to identify areas of common deficiency.

    Areas Covered in the Seminar:

    - Differences between drugs and cosmetics.
    - Good Manufacturing Practice (GMP).
    - Role of quality Assurance in the manufacturing process.
    - Responsibilities of management in FDA compliance.
    - Education of employees on GMPs and complaint handling.
    - Activities that are common to manufacturing processes.
    - State Health Departments and their relationship with FDA.
    - Case study on the manufacture of a cosmetic from raw materials to sale.
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