- 国家药品监督管理局
反映国家药监局机关和直属单位党员干部违纪问题 请寄：国家药监局机关纪委 地址：北京市西城区北露园1号
- NMPA - National Medical Products Administration
The National Medical Products Administration (NMPA) held a meeting on June 9 to conduct the 2024 annual review of the quality management system (QMS) in vaccine regulation and pharmaceutical manufacturing inspection
- China National Medical Products Administration (NMPA)
NMPA oversees standards setting, registration, and quality management of drugs, cosmetics and medical devices, as well as post-market inspection and risk management and registration of licensed pharmacists
- Understanding Chinese Authority NMPA
In 2018 National Medical Products Administration (NMPA, Chinese:国家药品监督管理局) replaced former China food and drug administration (CFDA) As one part of State Administration for Market Regulation (SAMR) the NMPA is in charge of supervision of drug, medical device and cosmetics in China
- Understand China’s National Medical Products Administration
What is the NMPA The China Food and Drug Administration (CFDA), or the now National Medical Products Administration (NMPA), is the Chinese regulating body that oversees pharmaceuticals, medical devices, and cosmetics Some of their tasks and responsibilities include: To routinely check the safety of the products offered in the market
- NMPA CHINA - New Drug Approvals
In its first incarnation as the CFDA, the NMPA replaced a large group of overlapping regulators with an entity similar to the Food and Drug Administration of the United States, streamlining regulation processes for food and drug safety
- China’s National Medical Products Administration (NMPA) - Asia Actual
The NMPA is based in Beijing and overseas the regulation of drugs, medical devices (including IVDs), and cosmetics They regularly issue new notices, draft guidance, regulations, and compulsory standards on their website ( EN CN )
- NMPA Medical Devices regulation - China Med Device
The NMPA issued the “Regulation on the Supervision and Administration of Medical Devices” on January 7, 2025, a revised version of the same-named regulation implemented on June 1, 2021
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