Cina Cosmetici

Cina Cosmetici

Evaluation of Cosmetic Efficacy Claims

I. Core Responsibilities and Procedures At the time of registration or notification, cosmetic registrants and notifiers must upload a summary of the basis for product efficacy claims to the specialized website designated by the National Medical Products Administration (NMPA). The registrant or notifier is responsible for the scientific validity, authenticity, reliability, and traceability of the submitted summary. Cosmetic efficacy claims must be supported by sufficient scientific evidence. This evidence includes scientific literature, research data, or the results of cosmetic efficacy evaluation tests. The methods used for evaluation must be scientific, reasonable, and feasible, and they must fulfill the purpose of the evaluation. Registrants and notifiers may conduct the evaluations themselves or entrust an evaluation balanced with appropriate capabilities to follow the requirements listed in Table 1. A summary of the efficacy claim basis will then be prepared and published based on the evaluation conclusions. II. Specific Evaluation Requirements by Category […]

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Cina Cosmetici

Compliance Guide for Cosmetic Safety Assessment

I. Key Dates and Scope II. Qualifications for Safety Assessors Cosmetic safety assessors must meet the following requirements: III. The Four-Step Risk Assessment Process The risk assessment for ingredients and substances involves these four steps: IV. Core Principles for Assessment 1. Ingredient Assessment 2. Product Assessment V. Testing for Harmful Substances VI. 2024 Update: How to Submit Reports Cosmetics are now divided into two categories for submission: VII. Record Keeping Safety assessment records must be kept for at least 10 years after the expiration date of the last batch of the product sold. Have Questions?

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Cina Cosmetici

NIFDC Solicits Public Comments on Six Microbiological Testing Methods for Cosmetics

To all relevant organizations: To further improve the technical standards for cosmetics, the National Institutes for Food and Drug Control (NIFDC) has organized the development and revision of six cosmetic standard drafts for public comment, including the General Rules for Microbiological Testing Methods in Cosmetics (Attachments 1–6). We are now formally soliciting public feedback. Please submit your comments through the “Cosmetic Standard Development and Revision Management System” (https://www.nifdc.org.cn/nifdc/bshff/hzhpbzh/hzhpbzhxt/index.html) as required. The deadline for submission is March 22, 2026. Attachments: National Institutes for Food and Drug Control (NIFDC) February 6, 2026 Have Questions?

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Cina Cosmetici

NIFDC Solicits Public Comments on Three Cosmetic Standards

To all relevant organizations: To further improve the technical standards for cosmetics, the National Institutes for Food and Drug Control (NIFDC) has organized the development and revision of three cosmetic standard drafts for public comment, including the Testing Method for Trivalent Chromium and Hexavalent Chromium in Cosmetics (Attachments 1–3). We are now formally soliciting public feedback. Please submit your comments through the “Cosmetic Standard Development and Revision Management System” (https://www.nifdc.org.cn/nifdc/bshff/hzhpbzh/hzhpbzhxt/index.html) as required. The deadline for submission is February 24, 2026. Attachments: National Institutes for Food and Drug Control (NIFDC) January 15, 2026 Have Questions?

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Cina Cosmetici

NMPA Solicits Public Comments on the Provisions on Management of Cosmetic New Ingredient Registration and Notification Dossiers

To further deepen regulatory reform, support innovation in cosmetic ingredients, and optimize the requirements for new ingredient registration and notification dossiers, the National Medical Products Administration (NMPA) has drafted the “Provisions on Management of Cosmetic New Ingredient Registration and Notification Dossiers (Revised Draft for Comments)” (Attachment 1). This draft was developed in accordance with the Cosmetic Supervision and Administration Regulation (CSAR), the Administrative Measures on Cosmetic Registration and Notification, and other relevant regulations, while considering the current state of industry development. We are now formally soliciting public feedback. The public comment period is from December 26, 2025, to January 25, 2026. Please provide your comments and suggestions by completing the Feedback Form (Attachment 2) and sending it to the following email address: hzpjgyc@nmpa.gov.cn. Please indicate “Feedback on Provisions on Management of Cosmetic New Ingredient Registration and Notification Dossiers” in the email subject line. Attachments: General Affairs Department of the NMPA

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