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WebMar 20, 2024 · The NMPA, formerly known as the China Food and Drug Administration, reviews and approves clinical trial applications for drugs to be registered in China. For a global biopharmaceutical company, the first step in China’s IND application process is a communications meeting with the NMPA’s Center for Drug Evaluation. NMPA uses the … WebNational Institutes for Food and Drug Control Chinese Pharmacopoeia Commission Center for Drug Evaluation of NMPA Center for Food and Drug Inspection of NMPA Center for … Provisions for Administration of Medical Device Recall. 2024-10-25. Promulgated … 不超过150个字符. Li Bo. Director for Drug Safety of NMPA. Director General of … NMPA Announcement on Updating the Catalogue of Raw Materials Banned for … Notice of the Center for Drug Evaluation of NMPA on the Applicability of E2B (R3) … China will downgrade its COVID-19 insurance reimbursement management … NMPA Notice on Matters Concerning the Registration of Drug-device Combination … Q&A on COVID-19 reinfection. 2024-12-29. The more virulent Delta strain of COVID … 不超过150个字符. (1) To supervise the safety of drugs (including traditional … Department of Comprehensive Affairs, Planning, and Finance Affairs. 2024-07 … churchill tank mk iii
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