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英文字典中文字典相关资料:


  • NMPA Roundup May 2026 - China Med Device
    Here’s the latest NMPA regulatory and clinical affairs news for medical device and IVDs pros in May 2026, presented by China Med Device
  • NMPA Roundup March 2026 - China Med Device
    Here’s the latest China NMPA regulatory and clinical affairs news for medical device and IVDs pros in March 2026
  • Appendix: New drugs approved by the NMPA in 2025
    Comprehensive list of new drugs approved by China’s NMPA in 2025, including chemical and biologic therapies, targets, disease indications, and approval dates
  • 2025 NMPA Approvals: China Clears Record Number of New Drugs
    With the tremendous development of China’s innovative drug industry as backdrop, 2025 saw the number of new drugs approved by the National Medical Products Administration (NMPA)—the country’s regulatory authority—reach triple digits for the first time, an increase that was driven primarily by therapies developed domestically
  • NMPA Biological Evaluation - China Med Device
    The National Institutes for Food and Drug Control of NMPA released the draft GB T 16886 1-2025, “Biological Evaluation of Medical Devices — Part 1:
  • New Drug Approvals in China in 2021 - DIA Global Forum
    The number of new drug approvals in China set a new record high in 2021 A total of 61 new drugs were approved by the National Medical Products Administration (NMPA), up from 46 in 2020 “New drug” is defined in this article as new chemical drugs or new biological products approved for the first time in China, excluding any new indications, new dosage forms, or new combination of approved
  • China NMPA Registration Questions - China Med Device
    What is China NMPA registration and classification system for medical device and IVD? The classification of medical device determines documentation required for China NMPA registration NMPA categorizes medical devices (including IVDs) into three classes (from I to III) based on their risk levels, as Class I being the lowest risk and Class III being the most complex and of highest risk Class
  • China GVP: Lifecycle Pharmacovigilance and Patient Safety
    In May 2021, the National Medical Products Administration (NMPA) in China issued an announcement about Good Pharmacovigilance Practice (NMPA Decree No 65 2021), hereafter referred to as GVP, the first pharmacovigilance guideline issued in accordance with China new Drug Administration Law of the People’s Republic of China
  • NMPA DEVICE STANDARDS 2026 - China Med Device
    NMPA issued the “2026 Medical Device Industry Standards Revisions Plan" It includes One mandatory and seventy-nine recommended standards
  • NMPA Moves ICH E2 Forward in China - DIA Global Forum
    Over the past two years, the Chinese National Medical Products Administration (NMPA) has aggressively implemented a series of ICH E2 guidances





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