NEWS

• For medical device products that require clinical evaluation, it is necessary to proceed from the company's own situation, fully consider the availability of resources, and select a reasonable clinical evaluation path according to product characteristics, clinical risks, existing clinical data, etc....

• Our company has already achieved ISO9001 , ISO13485, CE, certificate.With strong technolohgical power , state - of – the art management and strict quality control, our products have been will accepted by our global customers.

• Judging from the comparison of the scale of the medical device market and the pharmaceutical market, the global medical device market is roughly 33% of the global pharmaceutical market, and the proportion in my country is only 12%. According to statistics from the Firestone Creation Data Platform, a...

• Its use is aimed at preventing, diagnosing, treating, monitoring, and relieving diseases; diagnosing, treating, monitoring, relieving, and compensating for injuries or disabilities; and researching, replacing, regulating, and controlling anatomical or physiological processes. From the perspective of...

• The new version of the "Regulations on the Supervision and Administration of Medical Devices", which will be implemented on June 1, 2021, encourages innovation and promotes the high-quality development of the medical device industry is one of the highlights. This revision reflects the spirit of cont...

• Considering selling your medical device in China?? If so, you will need to register your medical device with China's regulatory agency, the National Medical Products Administration (NMPA). Below, let's take a look at the classification of China's medical device NMPA registration.First of all, accord...