EU CPNP, Announcement of regulatory revisions regarding CMR substances

On May 13, 2025, the EU announced an amendment to the European Council Regulation (EC) No 1223/2009 concerning the use of certain substances classified as carcinogenic, mutagenic, or toxic to reproduction (CMR) in cosmetic products. Annex II of the regulation contains the list of prohibited substances, while Annexes III to VI include substances that are restricted or permitted under specific co..

China NMPA, Announcement of the Quality Management Standards for Online Sales of Medical Devices

On April 28, 2025, the National Medical Products Administration (NMPA) of China released regulations outlining the basic requirements for the quality management of online sales of medical devices. These regulations specify the requirements that apply to online sellers and e-commerce platform operators selling medical devices online in China. The main contents of the regulation are as follows: ..