MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...

For instance, in October 2022, Freyr partnered with an orthopedic implant manufacturing company in Korea, and as per the agreement, provided it with regulatory device registration and legal ...

The MHRA has issued fresh guidance to help medical device manufacturers prepare for upcoming regulatory changes.

When conducting a clinical investigation, meeting regulatory requirements is predicated on factors such as the quality of ...

Apple is still facing headwinds in China. The company's overall sales in China declined 11.1% during to $18.51 billion during ...

A recent study identified 157 cardiovascular devices recalled from 2013 to 2022. Recalls were commonly attributed to device ...

For instance, in October 2022, Freyr partnered with an orthopedic implant manufacturing company in Korea, and as per the agreement, provided it with regulatory device registration and legal ...

For instance, in October 2022, Freyr partnered with an orthopedic implant manufacturing company in Korea, and as per the agreement, provided it with regulatory device registration and legal ...

The medical devices industry representatives said permitting such imports, despite the availability of similar products manufactured in India, threatened the efforts of Indian manufacturers to meet ...

and commentary on various regulatory challenges that exist in this area. Direct to device services are not entirely new; technology permitting direct communications between a satellite and a ...

Any radio frequency (RF) emitting devices, including those requiring International Mobile Equipment Identity (IMEI) registration, will not be permitted to operate unless registered with the ...