Medical Device Regulations
This paper explores the views of thought leaders on how registries can provide insight into the performance and safety of medical devices in the post Brexit landscape.
WILL MEDICAL DEVICE REGULATION STIFLE INNOVATION?
Sweeping regulations introduced by the Medicines and Healthcare products Regulatory Agency (MRHA) aims to improve safety.
Yet the more stringent legislation could make it tougher for manufacturers to introduce new devices in the market or the availability of more specialist ones.
As the future for medical device regulation continues to evolve, one outcome is certain. Medical device registries will have an increasingly important role to play in providing evidence for the safety of devices, and enabling clinicians to make informed decisions which best meet patients’ needs.
This paper explores the views of thought leaders on how registries can provide insight into the performance and safety of medical devices in the post Brexit landscape.
