GlobalData on MSN
Differing device regulation between regions causes trial challenges
Medical Devices includes a session from a regulatory expert on how companies can align their research between regions.
GlobalData on MSN
FDA announces regulatory exemptions for ‘non-medical grade’ devices
FDA commissioner Marty Makary revealed at the 2026 CES trade show in Las Vegas that low-risk devices will face less ...
The U.S. Food and Drug Administration says it will ease regulatory requirements for certain consumer wearable health devices.
FDA plans limited regulation of wearable medical devices, boosting Apple, Fitbit, Oura stocks as 50% of Americans use fitness ...
DUBLIN--(BUSINESS WIRE)--The "The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation) Training Course" ...
As we anticipate the upcoming annual PDA Universe of Pre-Filled Syringes and Injection Devices Conference in Phoenix this 22-23 October, we caught up with a member of the planning committee to get a ...
The rise of AI in health care presents new challenges related to the patentability and regulation of AI-driven medical technologies. This article examines the 2024 guidelines from the U.S. Patent and ...
SPE/MPD MiniTec conference at MD&M West features medical polymer innovations, sustainability keynote, and device design ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results