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NMPA issued the Announcement on Adjusting the Relevant Matters Concerning the Definition of the Attributes of Drug/Device Combination Products
2019-05-31
To further standardize the definition of the attributes of Drug/Device Combination Products, according to the Three- Determinations (of posts, duties and staffing) regulations for NMPA institutions, on May 31, 2019, NMPA announced the relevant matters as follows.
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NMPA Issued 3 Guidelines for Technical Review of the Registration of Synthetic Resin Teeth and Others
2019-05-22
To strengthen the supervision and guidance over the registration of medical device products and further improve the quality of registration review, NMPA organized the formulation of and published the Guidelines for Technical Review of the Registration of Synthetic Resin Teeth,the Guidelines for Technical Review of the Registration of IUD, and the Guidelines for Technical Review of the Registration of Implantable Drug Delivery System on May 22, 2019.
