The FDA and Cosmetic Oversight- What does that look like?

Schedule Thursday, March 7, 2024 || 10:00 AM PST | 01:00 PM EST
Duration 90 Mins
Level Basic & Advanced
Webinar ID IQW24C0357

Introduction to Cosmetics and their Regulation:

  • Definition and purpose of cosmetics
  • Overview of the FDA's role in cosmetic regulation
  • Understanding the Federal Food, Drug, and Cosmetic Act- focusing on the new Modernization of Cosmetics Regulation Act of 2022 (MoCRA)

FDA Regulations and Requirements for Cosmetics:

  • Labelling requirements for cosmetics, including ingredient listing and claims.
  • Safety considerations and prohibited/restricted ingredients.
  • Good Manufacturing Practices (GMPs) for cosmetic manufacturers

Cosmetic Safety and Adverse Event Reporting:

  • The FDA's approach to ensuring cosmetic safety.
  • Cosmetic Ingredient Review (CIR) process and ingredient safety assessments
  • Adverse event reporting requirements for cosmetic manufacturers
  • FDA's actions in response to reported safety concerns.

Challenges and Concerns in Cosmetic Oversight:

  • Product safety concerns in the cosmetic industry
  • Contamination, mislabeling, and deceptive marketing practices
  • Implications of counterfeit and adulterated cosmetics

Consumer Awareness and Trust:

  • Importance of consumer education in cosmetic use
  • Identifying safe and reliable cosmetic products
  • Building consumer trust through transparency and responsible marketing

Resources for Staying Informed:

  • Available resources for staying updated on cosmetic regulations.
  • Professional development opportunities in the cosmetic industry
  • Continuing education and staying informed about regulatory changes

These areas provide a comprehensive coverage of the FDA's oversight of cosmetics, regulatory requirements, safety considerations, emerging trends, challenges, and the importance of consumer awareness. Participants will gain a thorough understanding of the topic and its implications for the cosmetic industry.

Overview of the webinar

"The FDA and Cosmetic Oversight - What does that look like?" is a training session aimed at providing participants with an understanding of the role of the Food and Drug Administration (FDA) in regulating cosmetics. The training covers various aspects, including the definition and purpose of cosmetics, the FDA's authority and responsibilities, regulatory requirements, safety considerations, and emerging issues in the cosmetic industry.

The training begins with an introduction to cosmetics, highlighting their purpose and the different types available. It emphasizes the benefits and potential risks associated with cosmetic usage and addresses common misconceptions and industry challenges.

Participants then learn about the FDA's role in cosmetic oversight. This includes an overview of the FDA's authority, the impact of the Federal Food, Drug, and Cosmetic Act, - focusing on the new Modernization of Cosmetics Regulation Act of 2022 (MoCRA) and the limitations of the FDA's regulatory power.

The training will explore Good Manufacturing Practices (GMPs) for cosmetic manufacturers. The safety of cosmetics and adverse event reporting are discussed, including the Cosmetic Ingredient Review process and the FDA's actions in response to reported safety concerns. The training also addresses challenges and concerns in cosmetic oversight, such as product safety, contamination, mislabeling, and deceptive marketing practices.

Who should attend?

  • Cosmetic manufacturers and brand owners
  • Regulatory affairs professionals in the cosmetic industry
  • Quality assurance and quality control personnel
  • Product development and formulation scientists
  • Marketing and sales professionals in the cosmetic industry
  • Retailers and distributors of cosmetic products
  • Cosmetic industry consultants and advisors
  • Professionals involved in cosmetic ingredient sourcing and supply chain management.
  • Researchers and scientists studying cosmetics.
  • Compliance officers in the cosmetic industry

Why should you attend?

Understanding Regulatory Requirements: Attending this training will provide participants with a comprehensive understanding of the FDA's regulatory requirements for cosmetics. They will learn about labelling, ingredient listing, claims, and safety considerations, enabling them to ensure compliance and avoid regulatory issues.

Ensuring Product Safety and Quality: Participants will gain insights into the FDA's approach to ensuring the safety and quality of cosmetic products. They will learn about ingredient safety assessments, adverse event reporting, and the FDA's actions in response to reported safety concerns. This knowledge will help participants prioritize consumer safety and produce high-quality cosmetics.

Compliance and Risk Management: By attending this training, individuals in the cosmetic industry can stay updated on the latest regulatory changes and requirements. This will help them mitigate risks associated with non-compliance, such as product recalls, penalties, and legal issues. It will also enable them to make informed decisions and navigate the complex regulatory landscape more effectively.

Consumer Trust and Reputation: Understanding the FDA's oversight of cosmetics is essential for building consumer trust and maintaining a positive reputation in the industry. Consumers are increasingly concerned about the safety and efficacy of cosmetic products. By attending this training, industry professionals can demonstrate their commitment to compliance, product safety, and transparency, thereby enhancing consumer trust.

Personal and Professional Development: Enhancing knowledge of cosmetic oversight can contribute to personal and professional development. It enables individuals to expand their skill set, stay updated on industry best practices, and advance their careers in the cosmetic industry. Continuous learning is key to success in any dynamic and regulated field.

In summary, attending this training on FDA and cosmetic oversight is beneficial for industry professionals as it provides a deep understanding of regulatory requirements, helps ensure product safety and quality, supports compliance and risk management, builds consumer trust, keeps up with emerging trends, facilitates networking, and promotes personal and professional development.

Faculty - Miss.Meredith Crabtree

Meredith Crabtree has over 25 years’ experience in regulated industries ranging from Pharma, Medical Device, Biologics, Laboratory testing, Cosmetics, and Supplements. She has worked in both manufacturing and distribution as well as Human Health and Animal Health. Meredith currently works as a Quality Consultant performing label reviews, 3rd party inspections, Consent Decree and Recall support. She also performs regulatory assessments and Quality  training. Meredith has a degree in Medical Technology and is currently obtaining a degree in Quality Systems.

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