Understanding China’s Latest Cosmetic Regulations: Key Changes and Analysis of Non-compliance Cases


China\’s updated Cosmetic Supervision and Administration Regulation (CSAR) in 2021 has brought significant changes in the cosmetic industry. Stricter requirements have been implemented, such as product safety assessment, efficacy evaluation, adverse reaction monitoring, and ingredient safety information submission. Additionally, new requirements for cosmetic label management, online sales, and sample retention have been introduced. It is imperative for businesses to stay informed and comply with these regulations to ensure the safety and efficacy of their products.

With two and a half years of implementation, what is the current situation of cosmetic supervision under the CSAR framework? What are the key requirements affecting businesses in the subsidiary regulations? What are the common reasons for non-compliance of enterprises? To address these questions, ChemLinked organized this webinar that provides a detailed account of the current supervision situation, the key regulatory requirements and changes under the CSAR regulatory framework, and an analysis of non-compliance cases. Join us to stay informed and compliant with the regulations to avoid penalties and ensure product safety and efficacy.

Notes:

  • Please feel free to send us questions before, during or after the webinar;
  • The presentation deck and recording video will be uploaded to this webpage after the webinar;
  • If you can\’t attend the live webinar, register anyway and we will send you the webinar materials as soon as they’re available.

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Content


1. Status Quo of Cosmetic Supervision under CSAR Framework

1) Regulatory Framework for Cosmetics

2) Number and Types of Cosmetics Notified in 2022 and 2023

2. Key Regulations under CSAR Framework: Brief Introduction and Main Changes

1) Label Management

  • Key changes, small packaging labeling, children\’s cosmetics logo, and noteworthy points

2) Efficacy Evaluation

  • Evaluation requirements, controversial efficacy claims, efficacy evaluation methods

3) Ingredient Safety Information Submission

  • Submission methods, required information, Technical Guidelines for Filling in and Submitting Safety Information of Cosmetic Ingredients

4) Safety Assessment

5) Adverse Reaction Monitoring

  • Adverse reaction collection process

6) Good Manufacturing Practices

  • Sample retention management

7) Online Sales Management

8) Compliance Recommendations

3. Analysis of Non-Compliance Cases

1) Lack of Efficacy Evaluation Basis

2) Implied Medical Effect

3) Incomplete Notification Document

4) General Cosmetics Claiming Efficacy of Special Cosmetics

5) False Claims

6) Non-compliant Labeling

7) Absence of Person in Charge of Quality and Safety

8) Sales of Expired Cosmetics

9) Cosmetic Formula Inconsistent with Registration and Notification Documents

Schedule


Date Time (GMT+8) World Clock Language
2023-06-19 22:00 ~ 23:00 London: 15:00-16:00

New York: 10:00-11:00

English

Speaker


Hedy He

ChemLinked Regulatory Analyst

Hedy is an experienced cosmetic regulatory analyst in the ChemLinked team. She focuses on tracking, analyzing, and interpreting the latest cosmetic regulatory and market changes in China, Indonesia, Vietnam, and the rest of the Asia Pacific area. With an in-depth understanding of cosmetics regulations, she attended various industry conferences and presented several speeches at multiple industry conferences such as In-cosmetics Asia and has often been interviewed by well-known cosmetics industry media. Area of expertise: China cosmetic import compliance, pre-market approval procedures, animal testing, Indonesia cosmetics halal certification, and Vietnam cosmetics compliance.

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