Parliamentary panel report calls for overhaul of medical device regulatory procedures to enhance transparency and sector ...

Under IVDR, clear and specific IVD intended use criteria are required and introduce significant challenges for manufacturers ...

The Indian government is considering lowering tariffs on US medical devices to mitigate potential US tariff threats on Indian ...

XBeta founder Frederick Kruger offers advice for medical device startups based on his firm's development of the Spiro Wave ...

Manufacturers urge the govt to review medical device tariffs as the Centre considers cutting import duties on them in India.

Expanding the use of e-bikes in Oregon is “really one of those win-win-win kinds of solutions,” said Rep. Mark Gamba, a Democrat from Milwaukie and e-bike user. “It gives people a dependable, ...

Manufacturing engineers are the background force behind successful medical device coatings, ensuring precision, consistency, ...

A quality management system (QMS) can often become bloated and unwieldy. This expert helps you understand key QMS basics and ...

India's medical device industry urges government to reconsider tariff reduction on US imports, citing concerns over market ...

To avoid overlaps, the industry is calling for aligning MDR/IVDR with the EU's digital frameworks, pharmaceutical regulations, and clinical trial regulations.

The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", ...

The regulatory environment for prescription medical device manufacturers and distributors has become increasingly stringent as state-based ...