The US Food and Drug Administration (FDA) hold cosmetic manufacturers and distributors responsible for the safety and quality of their cosmetics. This webinar serves to guide cosmetic manufacturers and distributors as well as other entities such as color additive manufacturers and analytical and microbiological laboratories on FDA recommendations and requirements concerning the safety and quality testing of cosmetics. Topic areas covered in this webinar include, FDA considerations for microbiological testing, animal testing, potential contaminants, nanomaterials in cosmetics, cosmetic good manufacturing practices (GMP) compliance testing, shelf life/expiration dating, select cosmetic ingredients and color additive batch certification.
Why Should You Attend:
FDA periodically analyzes cosmetics, especially if aware of a potential problem. The information obtained can be used to alert consumers, support regulatory actions. To avoid action from the regulatory body. Cosmetic manufacturing companies should test the cosmetic product before it start selling the product. Attend this cosmetic safety training to learn different types of cosmetic testing which are practiced in the cosmetic industry to achieve compliance with the US FDA.
Areas Covered in this Webinar:
Microbiological Testing for cosmetics
Animal Testing & Cosmetics
Color Additives & Batch Certification
Select Cosmetic Ingredients: Prohibited & Restricted Ingredients
Shelf Life/Expiration Dating
Nanomaterials in Cosmetics
Cosmetic Good Manufacturing Practices (GMP) Compliance Testing
To ensure safety and quality of a cosmetic/cosmetic ingredient and achieve compliance with the US FDA
Who Will Benefit:
Cosmetic Ingredient Manufacturers
Color Additive Manufacturers
Analytical & Microbiological Laboratories involved in Cosmetic / Cosmetic Ingredient Testing
Rachelle D’Souza, CEO of Regulatory Heights Inc., has successfully licensed various medical and consumer products and facilities with international regulatory authorities / agencies for multinational and start-up companies.
Her expertise also includes clinical trial master file documentation, and the design and maintenance of globally compliant quality, safety / pharmacovigilance and medical information systems.
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