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The 2023 medical device industry standard formulation and revision plan project release

Standard / By

On May 24, the General Department of the NMPA issued a notice on printing and distributing the 2023 medical device industry standard formulation and revision plan: In order to implement the “Implementation Opinions on Comprehensively Strengthening the Construction of Drug Supervision Capabilities” issued by the General Office of the State Council and the relevant requirements …

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Guidelines for Medical Device Registration Review in 2023 Prepare Plan

Guidelines / By

Formulation plan for guiding principles for registration review of Class III medical devices In order to further strengthen the guiding role of the guiding principles for medical device registration review in the registration application and technical review work, the CMDE organized and drafted a compilation plan for the guidelines for medical device registration review, which …

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Aliquam Eleifend Nulla Posuere Sollicitudin

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Diam maecenas ultricies mi eget mauris pharetra et ultrices neque. Purus non enim praesent elementum. Commodo ullamcorper a lacus vestibulum sed arcu non odio. Platea dictumst quisque sagittis purus sit amet volutpat consequat. Odio facilisis mauris sit amet. At imperdiet dui accumsan sit amet. Vehicula ipsum a arcu cursus. Scelerisque mauris pellentesque pulvinar pellentesque habitant …

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Consequat Interdum Varius Amet Mattis Vulputate

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Massa placerat duis ultricies lacus sed turpis tincidunt id aliquet. Venenatis tellus in metus vulputate eu scelerisque felis imperdiet. Aliquam sem et tortor consequat id porta nibh. Tempor orci eu lobortis elementum nibh tellus. Quisque sagittis purus sit amet volutpat consequat mauris. Accumsan tortor posuere ac ut consequat semper viverra nam. Vel pretium lectus quam …

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