Industry consultant Michael Drues will discuss how medical device companies can better prepare for FDA inspections.

The European Union’s Medical Device Regulation (MDR) is a complex regulatory framework created to put in place rules and requirements in how medical devices are designed, manufactured, and marketed.

In the United States, medical device regulation and intellectual property (IP) protection are governed by complex statutory and regulatory frameworks that are distinct from—but closely related to, and ...

DONGGUAN, GUANGDONG, CHINA, January 15, 2026 /EINPresswire.com/ -- As global healthcare regulations tighten and patient ...

Ambient Voice Technology (AVT) has seen a rise of popularity in clinical settings, mainly due to its potential to ease administrative burden by transcribing, and in some cases summarizing ...

The "Medical Device Regulations in the Middle East and North Africa Training Course (May 18th - May 19th, 2026)" has been added to ResearchAndMarkets.com's offering. The size of the medical device ...

Dublin, Dec. 23, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Regulations in Asia-Pacific Markets Training Course (Mar 3rd - Mar 4th, 2026)" training has been added to ResearchAndMarkets.com's ...