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[Updated] South Korea Issues the Guideline on Reporting Functional Cosmetic
Dec 02, 2022
South Korea unveiled a notice to solicit public opinion on the new Guideline on Submission of Reporting Functional Cosmetic. The Guideline drafts the procedures to submit the report and the instructions for filling in the report for different situations.
South Korea Pre-market Approval Efficacy
NEWS

Australia Adopts Rules for Chemical Introductions at Low Volumes (Updated on Nov 25, 2022)
Nov 30, 2022
On September 26, 2022, the Australia Government released a public invitation for comments on the Industrial Chemicals (General) Amendment (Introductions of 10 kg or Less) Rules 2022, which would provide more reasonable and appropriate requirements for certain lower risk chemical introductions at low volumes in a registration year. The public consultation will end on October 11, 2022.
Australia Pre-market Approval Ingredients
FAQ

FAQs Vol. 14 | Guangzhou AMR Answers Questions About Cosmetic Notification and Labeling Requirements
Nov 28, 2022
Guangzhou Administration for Market Regulation (AMR) released several FAQs to answer questions that companies have encountered in complying with the cosmetic notification and labeling requirements. ChemLinked will keep updating new FAQs. Please stay tuned to get the updates.
Chinese Mainland Pre-market Approval Labeling/Claim/Advertising Post-market Surveillance
NEWS

[Updated] China Cosmetic and New Cosmetic Ingredient Notification: The Current Situation
Nov 18, 2022
China implemented a notification system for general cosmetics and low-risk new cosmetic ingredients. ChemLinked summarized the current situation of cosmetic and new cosmetic ingredient notification.
Chinese Mainland Pre-market Approval Ingredients CSAR New Ingredient Management
NEWS

China NIFDC: Advertising “Ingredient Submission Code Obtained” Suspected of False or Exaggerated Publicity
Nov 14, 2022
On October 27, 2022, China National Institutes for Food and Drug Control (NIFDC) released an announcement answering a question related to the generation of cosmetic ingredient submission code. It emphasizes that using terms such as "ingredient submission code obtained" to falsely claim that the ingredients have been approved or recognized by regulatory authorities is suspected of false or exaggerated publicity, and will be investigated and punished.
Chinese Mainland Pre-market Approval Labeling/Claim/Advertising CSAR Enterprise Obligations
NEWS

Indonesia Consults on the Amendments to Required Documents for Product Information File (PIF)
Nov 11, 2022
The draft of the Guidelines for Product Information File (PIF) clarifies the standards for documents included in PIF, and amends the documents required in PIF.
Indonesia Pre-market Approval
NEWS

Indonesia Implements the Amended Procedure for the Submission of Cosmetics Notification
Nov 09, 2022
On Dec. 6, 2021, Indonesia Food and Drug Supervisory Agency (BPOM) issued a revised draft of the Procedure for Submission of Cosmetics Notification for public consultation. On Oct. 5, 2022, Indonesia issued and implemented the revised Procedure for Submission of Cosmetics Notification, replacing the 2020 version.
Indonesia Pre-market Approval
NEWS

Thailand Issues Amendments to the Cosmetic Act B.E. 2558 (2015)
Nov 09, 2022
On October 12, 2022, Thailand published the Cosmetics Act (No. 2) B.E. 2565 (2022) in the Government Gazette (Vol. 139, Chapter 63) to amend the existing Cosmetic Act B.E. 2558 (2015) ...
Thailand Pre-market Approval Post-market Surveillance
RECAP

Monthly Recap: Global Cosmetic Regulatory Updates | October 2022
Nov 04, 2022
ChemLinked rounded up the global regulatory updates on cosmetic products in October...
Chinese Mainland Taiwan, China South Korea Japan Indonesia Philippines Thailand Australia AP Pre-market Approval Ingredients Labeling/Claim/Advertising Post-market Surveillance Entry-exit Efficacy Animal Testing Testing GMP UK EU Middle East
NEWS

[Updated] Philippines to Modify the Requirements for Licensing and Inspection of Health Products, Cosmetics Included
Oct 13, 2022
On May 27, 2022, Philippines FDA issued a draft of Updated Guidelines on licensing and inspection of health products. Compared to its predecessor, AO No. 2020-0017, the Updated Guidelines further clarifies the qualification for the qualified person, supplements requirements for LTO application, and devises a more comprehensive plan to regulate inspection.
Philippines Pre-market Approval Enterprise Obligations

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