Lobby Letter to National Medical Product Administration (NMPA) about feedbacks and suggestions on raw material safety information submission, product supplementary information submission requirement

2022-03-23 | Beijing

Recently, in the process of discussing the new regulations and actively implementing the requirements, members of the Cosmetics Working Group of the European Chamber have identified some ambiguities and challenges at the implementation level. European Chamber has provided feedback on several present major issues of greatest urgency and concern to foreign cosmetic companies, including specific issues and suggestions related to the raw material safety information submission, and completing the document supplementation replenishment and requirements change of previously registered and notified cosmetics.