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Medical Device

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  • 2014.09.19.FRI

    Other MD Matters

    Fei Li

    Medical Devices Registration Administration Method (hereinafter referred to as "the Method") is the core regulation for standardize the registration of medical devices. The Method has been fully demonstrated, it has been published since 30th July and put into enforcement since 1st October 2014.

  • 2014.06.23.MON

    Other MD Matters

    Fei Li

    As the development of economy and medical devices industry, Regulations on Supervision and Administration of Medical Devices implemented since April 1st, 2000 are no longer able to play a satisfactory role in classification, strengthening manufacturer's responsibility, punishing illegal activities and etc. After repeating research, argument and revision in 6 month, the new Regulations on Supervision and Administration of Medical Devices (hereinafter referred to as 'the new regulation') has been issued at March 31st and will be put into implementation from June 1st.

  • 2014.05.07.WED

    Other MD Matters

    Fei Li

    As social economy, especially medical devices industry develops, medical devices registration administration system improves continuously. The State Council of the People's Republic of China issued "Regulations on Supervision and Administration of Medical Devices"(Decree of the State Council of the People's Republic of China No. 276) in January 2000, and it has been implemented since April 1st, 2000. This means supervision and administration of medical devices in China have entered a new stage, in addition the regulation system and operation system of medical devices registration administration were established and improved continuously, which would help to ensure the safety and efficacy of using medical devices and promote the healthy development of medical devices industry.

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