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The National Drug Administration has issued guidance on strengthening the hierarchical supervision of medical device production and operation

On September 9th, the National Drug Administration issued the "Guiding Opinions on Strengthening the Grading Supervision of Medical Device Production and Operation" (hereinafter referred to as the "Guiding Opinions"), guiding drug regulatory departments in various regions to better carry out the supervision of medical device production and operation under the medical device registration system.

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2022

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09

UDI enables Digital transformation of medical device industry

On December 10, 2019, the Medical Device Unique Identification Database (UDID) organized and constructed by the National Drug Administration was officially launched and put into operation. In the past three years, with the strong support and joint efforts of all parties

23

2022

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09

Investment opportunities in the medical device industry

In the past decade, the US stock market has produced a total of 14 medical stocks with a market value of over 10 billion US dollars, of which 8 are medical devices, 3 are innovative drugs, and 3 are medical services. This indicates that medical device companies have high growth potential.

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2023

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