An Introduction to Upcoming Modernization of Cosmetics Regulation Act (MoCRA)
Possible Models for FDA GMP Regulations
![MoCRA Models FDA Draft GMP Guidelines MoCRA Models FDA Draft GMP Guidelines](https://easconsultinggroup.com/wp-content/uploads/2023/03/MoCRA-Models-FDA-Draft-GMP-Guidelines.png)
Existing FDA Draft Cosmetic GMP Guidelines
![MoCRA Models ISO Technical Committee 217 Standard 22716 MoCRA Models ISO Technical Committee 217 Standard 22716](https://easconsultinggroup.com/wp-content/uploads/2023/03/MoCRA-Models-ISO-Technical-Committee-217-Standard-22716.png)
ISO Technical Committee 217: Standard 22716
![MoCRA Models 21CFR211 MoCRA Models 21CFR211](https://easconsultinggroup.com/wp-content/uploads/2023/03/MoCRA-Models-21CFR211.png)
21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals
![MoCRA Models 2022 PCPC QA Guidelines MoCRA Models 2022 PCPC QA Guidelines](https://easconsultinggroup.com/wp-content/uploads/2023/03/MoCRA-Models-2022-PCPC-QA-Guidelines.png)
2022 PCPC Quality Assurance Guidelines
Cosmetics
EAS Consulting Group provides consulting services to the cosmetic industry, regulated under the authority of the Federal Food Drug & Cosmetic Act and the Fair Packaging and Labeling Act. Whether you need assistance with evaluating the safety of your formulation, label reviews, submission of a color additive petition, the Voluntary Cosmetic Registration Program, or determining if your product is a cosmetic, OTC drug or cosmetic/drug combination, EAS is here to help. While U.S. cosmetic products have no GMP requirements, it is imperative to ensure safe production and distribution, including co-packers, of these products.
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