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NEWS
China May Provide Six-month Transition Period for Submission of Cosmetic Safety Assessment Report (Full Version)
Mar 18, 2024
1) The regulatory authorities are developing and aiming to promptly publish optimization measures and technical guidance documents pertaining to cosmetic safety assessment; 2) Regarding the submission of full version of safety assessment reports, a six-month transition period is under consideration. Registrants and notifiers of cosmetic products that have already started safety assessments before May 1, 2024, will be allowed to submit a simplified version of the report within a specified timeframe.
Chinese Mainland
Pre-market Approval
Safety Assessment
CSAR
Enterprise Obligations
ANALYSIS
A Collection of China’s Non-compliant Cosmetics with Prohibited Ingredients, Maximum Penalties of 2.49 Million Yuan
Mar 18, 2024
According to data from National Medical Products Administration (NMPA), 88 batches of non-compliant products containing prohibited ingredients were detected between Jan. 2023 and Feb. 2024. Notably, 79 batches were identified in 2023, exhibiting a year-on-year surge of 155% compared to 2022.
Chinese Mainland
Post-market Surveillance
NEWS
[Updated] EU Amends the Use Requirements for 13 Nanomaterials in Cosmetics
Mar 15, 2024
On March 15, 2024, EU published a Commission Regulation aiming at revising the ingredient lists in Regulation (EC) No 1223/2009 (Cosmetics Regulation) regarding the use of nanomaterials in cosmetics. It will come into effect on April 4, 2024.
Ingredients
EU
NEWS
UK SAG-CS Releases the Opinion on Methyl Salicylate
Mar 15, 2024
On March 8, 2024, UK’s Scientific Advisory Group on Chemical Safety in Consumer Products (SAG-CS) introduced the final opinion on the use of Methyl Salicylate (CAS No. 119-36-8) in cosmetic products. This opinion establishes specific concentration limits for various product types and age groups.
Ingredients
UK
NEWS
Shanghai Government Clarifies Requirements for Cosmetics Advertising: Permissible Efficacy Claims, Content Requirements, and Prohibited Advertising Contents
Mar 14, 2024
The Guidelines provides clear guidelines on the obligations of cosmetic manufacturers and operators as well as necessary documentation for cosmetic advertising. It also specifies permissible efficacy claims, content requirements, and prohibited advertising contents.
Chinese Mainland
Labeling/Claim/Advertising
Post-market Surveillance
Enterprise Obligations
NEWS
[Updated] EU SCCS Releases the Final Opinion on Hexyl Salicylate
Mar 14, 2024
On March 11, 2024, EU SCCS issued the final opinion regarding the use of Hexyl Salicylate (CAS No. 6259-76-3) in cosmetics, which reaffirms the conclusion from the preliminary opinion.
Ingredients
EU
FAQ
FAQs Vol. 16 | Guangzhou AMR Explains New Cosmetic Ingredient Notification, Multi-shade Cosmetics Notification, and More
Mar 14, 2024
On February 20, 2024, Guangzhou Administration for Market Regulation (AMR) released a series of frequently asked questions (FAQs) related to new cosmetic ingredient notification, multi-shade cosmetics notification, eye irritation test, changes to notified information, and re-notification of previously cancelled products.
Chinese Mainland
Ingredients
Testing
NEWS
Japan Plans to Approve A New Ingredient for Rinse-off Hair Styling Products
Mar 13, 2024
On March 8, 2024, the Ministry of Health, Labour and Welfare of Japan released a proposal for the Standards for Cosmetics, inviting public consultation. The proposal requests the inclusion of "Cysteamine Hydrochloride". Any comments can be submitted before April 8, 2024.
Japan
Ingredients
RECAP
Monthly Recap: Global Cosmetic Regulatory Updates | February 2024
Mar 12, 2024
ChemLinked rounded up the global regulatory updates on cosmetic products in February...
Chinese Mainland
South Korea
Japan
India
Singapore
Thailand
Australia
Ingredients
Labeling/Claim/Advertising
Post-market Surveillance
Testing
NEWS
Indonesia BPOM Unveils the 2024 Legislative Plan, Involving Cosmetic Notification, Labeling, Ingredient Requirements, Adverse Reaction Monitoring, Contamination Limits
Mar 11, 2024
On March 1, 2024, the Indonesian Food and Drug Supervisory Agency (BPOM) released the 2024 legislative plan, including the finalized/draft version of amendments and new regulations.
Indonesia
Pre-market Approval
Ingredients
Labeling/Claim/Advertising
Post-market Surveillance
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