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Jarius Ji

ChemLinked Regulatory Analyst

Jarius is a cosmetic regulatory analyst in the ChemLinked team. She focuses on tracking and interpreting the latest cosmetic regulatory changes in China, Singapore, Philippines, and the rest of the Asia Pacific area.

Articles (66) Webinars (3)

[Updated] Philippines to Impose New Requirements on the PIF Audit for Cosmetic Products
Feb 01, 2023
Compared to the Circular No. 2018-001 currently in force, the Updated Guidelines adopts proper classification to present the previously included guidelines in a more clear and logical manner, and provides important supplements to PIF Audit.
Philippines Post-market Surveillance
EU SCCS Consults on Opinion as to Salicylic Acid
Dec 19, 2022
On December 15, 2022, EU Scientific Committee on Consumer Safety (SCCS) released the preliminary opinion on Salicylic Acid (CAS No. 69-72-7). The opinion is open for comments until February 17, 2023.
Ingredients EU
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
EU to Ban 30 More CMR Substances in Cosmetics from December 2023
Nov 22, 2022
On November 17, 2022, EU notified WTO of a draft Commission Regulation which proposed to newly include 30 more CMR substances into the prohibited ingredients list in Regulation (EC) No 1223/2009. The draft is currently open for comments until January 16, 2023, and will officially take effect from December 1, 2023.
Ingredients EU
[Updated] Import License for Dual-use Items and Technologies: A Must-have Ticket for Exporting Cosmetics Containing Triethanolamine (TEA) to China
Nov 18, 2022
For exporting cosmetics containing TEA to China, regardless of the concentration, it is mandatory to apply for the Import License for Dual-use Items and Technologies. It takes about one and a half months for the whole application process, whose valid period is not more than one year in general.
Chinese Mainland Ingredients Entry-exit
EU to Adopt Six Changes to the Use Requirements for Cosmetic Ingredients
Nov 16, 2022
On November 11, 2022, the EU introduced new amendments to the use requirements for cosmetic ingredients in Regulation (EC) No 1223/2009. All amendments aim at the lists of restricted ingredients and permitted UV filters, including adding two restricted ingredients and two permitted UV filters, and amending the use requirements for one restricted ingredient and one permitted UV filter.
Ingredients Labeling/Claim/Advertising EU
EU SCCS Finalizes the Scientific Advice on Triclocarban and Triclosan
Nov 10, 2022
On November 4, 2002, EU Scientific Committee on Consumer Safety (SCCS) released the final scientific advice on Triclocarban and Triclosan in cosmetics. Compared to the preliminary version released in this March, the final advice further clarifies the applicable consumers in different use conditions of these two ingredients, as well as additional concerns regarding their use in cosmetics.
Ingredients EU
EU SCCS Publishes the Revised Opinion on Vitamin A
Nov 08, 2022
On October 26, 2022, EU SCCS released the revised opinion on Vitamin A. In the revised opinion, SCCS reiterates the conclusion stated in SCCS/1576/16 that, vitamin A in cosmetics at the concentrations of 0.05% of retinol equivalent in body lotion, and 0.3% of retinol equivalent for other leave-on and rinse-off products is safe.
Ingredients EU
CSAR Subsidiary Regulations: China Finalizes Inspection Points and Judgment Principles of Cosmetic Good Manufacturing Practices
Nov 05, 2022
On October 25, 2022, NMPA released the finalized Inspection Points and Judgment Principles of Cosmetic Good Manufacturing Practices, which will take effect on December 1, 2022. Compared to the previous draft, the finalized Points adopts minor amendments.
Chinese Mainland GMP CSAR Enterprise Obligations
[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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