INSIGHTS

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NMPA Introduces New Measures to Support Innovation of Cosmetic Raw Materials

The National Medical Products Administration has issued an announcement on the release of several regulations to support the innovation of cosmetic raw materials.

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NMPA Guidelines for Submission of Cosmetics Safety Assessment, China Part III.6

This section outlines the comprehensive safety assessment requirements for cosmetic products in China.

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NMPA Guidelines for Submission of Cosmetics Safety Assessment, China, Part III.5

Outline the specific procedures and requirements for safety assessments of cosmetic products under special circumstances.

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NMPA Guidelines for Submission of Cosmetics Safety Assessment, China, Part III.4

Outline the procedures for safety testing when ingredient-level assessments are not feasible or complete.

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NMPA Guidelines for Submission of Cosmetics Safety Assessment, China, Part III.3

Outline safety assessment guidelines for specific cosmetic ingredients in China, focusing on special consideration due to unique properties or potential risks.

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NMPA Guidelines for Submission of Cosmetics Safety Assessment, China, Part III.1

Outline the general principles and self-inspection points for safety assessment reports.

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NMPA Guidelines for Submission of Cosmetics Safety Assessment China, Part I

Introduction of a comprehensive framework for evaluating and documenting the safety of cosmetic products in China.

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Regulation (EU) 2023/1545 – Update Labelling of Fragrance Allergens

Regulation (EU) 2023/1545 - Update Labelling of Fragrance Allergens

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Regulations on the management of registration and filing materials for new cosmetic raw materials

Outline the comprehensive requirements of the application process and post-market compliance for new cosmetic raw materials in China.

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Administrative Measures for Drug Registration

Outline comprehensive regulations for drug research, registration, and market authorization, ensuring safety, efficacy, and quality control across TCM, chemical drugs, and biological products.

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Specification for Hygienic Supervision of Disinfection Products

Outline comprehensive regulations for disinfectant manufacturers, importers, and users, emphasizing strict hygiene supervision to safeguard public health in the medical sector.

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Administrative Measures on Disinfection

Outline comprehensive regulations for disinfection management, product standards, and service providers, aiming to prevent infectious diseases and protect public health.

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Notice of the National Health and Family Planning Commission on Regulations on Hygiene and Safety Evaluation of Disinfection Products

A comprehensive framework for evaluating, classifying, and managing disinfection products.

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Management Practice for Labeling and Instructions of Disinfection Products

Provide comprehensive guidelines for labelling of disinfectants, ensuring product safety and efficacy through stringent regulatory oversight and standardized information disclosure

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Drug Administration Law of the People’s Republic of China

Provide a comprehensive framework for drug development, production, and distribution, emphasizing safety, efficacy, and accessibility while promoting innovation in both modern and TCM sectors.

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Regulations on the Administration of Drug Instructions and Labels

Provide regulatory standards for drug information disclosure, ensuring clear, accurate, and scientifically-backed instructions and labeling.

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