FDA's new Cosmetic labeling requirements
60 Minutes
The FDA recently published changes to Cosmetic Label requirements. This course will discuss the current FDA regulations for cosmetic products. Discussions will also include a historical timeline of FDA labeling oversight and why it is necessary. An overview of the challenges to meeting these requirements will be an additional talking point. This course will define what makes a product misbranded and/ or adulterated will be discussed as well as the consequences a facility will face if misbranded/ adulterated products enter the marketplace.
WHY SHOULD YOU ATTEND?
The FDA recently updated the regulations related to Cosmetic product labeling. This training will provide an overview of all the current requirements that must be followed to avoid misbranding and/ or adulterated products in the marketplace.
AREA COVERED
- What is a cosmetic?
- History of FDA Intervention in product labeling
- What makes a product deemed to be misbranded and/ or adulterated?
- Past regulations
- Current requirements by the FDA related to Cosmetic product labels.
- Challenges that facilities can face related to Cosmetic product labels.
- Consequences of nonconformance to labeling requirements.
LEARNING OBJECTIVES
- Define a cosmetic in terms of FDA regulations.
- Define and understand misbranded and/ or adulterated products.
- Awareness of label requirement changes
- Understand the FDA requirements for labeling Cosmetic products.
- Identify challenges that exist with the regulations surrounding Cosmetic labels.
- Be aware of the consequences of failure to label products according to FDA requirements
WHO WILL BENEFIT?
- Regulatory Affairs and Quality Managers
- Product Labeling personnel
- Product Managers
- Auditors
- Marketing Representatives
The FDA recently updated the regulations related to Cosmetic product labeling. This training will provide an overview of all the current requirements that must be followed to avoid misbranding and/ or adulterated products in the marketplace.
- What is a cosmetic?
- History of FDA Intervention in product labeling
- What makes a product deemed to be misbranded and/ or adulterated?
- Past regulations
- Current requirements by the FDA related to Cosmetic product labels.
- Challenges that facilities can face related to Cosmetic product labels.
- Consequences of nonconformance to labeling requirements.
- Define a cosmetic in terms of FDA regulations.
- Define and understand misbranded and/ or adulterated products.
- Awareness of label requirement changes
- Understand the FDA requirements for labeling Cosmetic products.
- Identify challenges that exist with the regulations surrounding Cosmetic labels.
- Be aware of the consequences of failure to label products according to FDA requirements
- Regulatory Affairs and Quality Managers
- Product Labeling personnel
- Product Managers
- Auditors
- Marketing Representatives
Speaker Profile
Meredith Crabtree
Meredith Crabtree has over 25 years’ experience in regulated industries, ranging from Blood, Plasma, Tissue, Laboratory, Pharma, Medical devices, Cosmetics, Supplements, and Animal Health manufacturing and distribution. Meredith 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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