Cosmetic
Tel: 0086 571 87206574
Email: service@cirs-group.com
Asia Pacific
China
China Cosmetic Registration and Filing
China New Cosmetic Ingredient Registration and Filing
China Disinfectant Notification
China Cosmetic Ingredient Quality and Safety Information Code Application
China Cosmetics Safety and Efficacy Test
China Cosmetic Safety Assessment Report
China Cosmetic Formula/Label/Claim Review
China Toothpaste Filing
South Korea
Cosmetics Notification in South Korea
Quasi-drug Products Registration in South Korea
Functional Cosmetics Notification in South Korea
Cosmetic GMP Consulting
Japan
ASEAN
Europe
European Union
Compliance with the EU Cosmetic Regulation
Claims and Warnings in the EU and the UK Cosmetic Regulations: A Comprehensive Guide to Compliance
Understanding Labeling Requirements for Cosmetics in the EU and the UK
How to Assess Product Safety according to EU and UK Cosmetic Regulations (CPSR)
Product Information File (PIF)
Responsible Person
United Kingdom
Regulatory News
MoreOn 13 January, 2025, the Scientific Committee on Consumer Safety (SCCS) of the European Union issued preliminary opinion (SCCS/1674/25) on Butylparaben (CAS No. 94-26-8). The deadline for comments is set for March 10, 2025.
On November 26, 2024, the US Food and Drug Administration (FDA) proposed establishing and requiring standardized testing methods for detecting and identifying asbestos in talc-containing cosmetic products, as mandated by the Modernization of Cosmetics Regulation Act of 2022 (MoCRA). This proposed rule, if finalized, would protect consumers by – to the extent it reduces exposure to asbestos – resulting in fewer asbestos-related illnesses.
This article compiles the cosmetic regulation updates that took place in November and December, covering regions and countries including Europe (EU, Austria, Russia), the Americas (USA, Canada), and the Asia-Pacific region (China, Thailand, Indonesia, Vietnam, Malaysia).
This article compiles data on cosmetic sampling inspections conducted within China and updates related information for December 2024.
On December 11, 2024, the US Food and Drug Administration (FDA) issued updated guidance for industry on the registration and listing of cosmetic product facilities and products. The guidance finalizes the frequently asked questions and answers (FAQ) in Appendix B (Q1-19). In addition, three new FAQs (Q20-22) in Appendix B of the guidance are marked as “for comment purposes only”. These three FAQs are available for comments until January 13, 2025.