The latest EU organization to be named under the Medical Device Regulation is based in Austria.
A new notified body, QMD Services, has been named which is headquartered in Vienna just a week ahead of MedTech Forum, the annual conference of MedTech Europe, in the Austrian capital.
The organization has been designated under the Medical Device Regulation (MDR) and is Austria’s first and only notified body under...
A government-backed program is working on improving the ability to run dementia clinical trials in the UK, and access to trials for participants.
Freespira’s device has been FDA-approved to treat panic disorders and PTSD. CEO Joe Perekupka told Medtech Insight the company’s innovative approach includes patient coaching, insurance partnerships to identify potential users, and lobbying for broader insurance coverage for digital therapeutics.
The US FDA posted three warning letters in July, covering medical supply kits, wearables and orthopedics.
