Cosmetic Testing for US FDA Compliance

Duration: 60 Minutes
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The US Food and Drug Administration (FDA) holds 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.
Cosmetic Testing
Instructor: Rachelle D'Souza
Product ID: 501764
Objectives of the Presentation
To ensure safety and quality of a cosmetic/cosmetic ingredient and achieve compliance with the US FDA, specifically by covering the following FDA topic areas:
  • Microbiological Testing for cosmetics
  • Animal Testing & Cosmetics
  • Potential Contaminants
  • Color Additives & Batch Certification
  • Select Cosmetic Ingredients: Prohibited & Restricted Ingredients
  • Shelf Life/Expiration Dating
  • Nanomaterials in Cosmetics
  • Cosmetic Good Manufacturing Practices (GMP) Compliance Testing
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 webinar to learn different types of cosmetic testing which are practiced in the cosmetic industry to achieve compliance with the US FDA.

Who will Benefit
  • Cosmetic Manufacturers
  • Cosmetic Distributors
  • Cosmetic Ingredient Manufacturers
  • Color Additive Manufacturers
  • Analytical & Microbiological Laboratories involved in Cosmetic / Cosmetic Ingredient Testing
$375
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  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
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Recorded Session - How it works
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  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Rachelle D'Souza has licensed various medical and consumer products and facilities for start-ups and multi-national 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

At Regulatory Heights Inc., Rachelle continuously monitors the current regulatory environment and utilizes regulatory intelligence as a strategic business driver for her clientele. Her numerous articles on the latest international regulatory developments have been published in print and on-line by regulatory professional associations and industry magazines around the world.

Her versatility has enabled Regulatory Heights Inc. to support companies, in particular, start-ups with the licensing of their drugs and medical devices in international markets like Canada, USA, EU, China, Japan, Australia and New Zealand.
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