Dublin, Sept. 24, 2025 (GLOBE NEWSWIRE) -- The "A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU (European Union) and UK Training Course (Oct 21, 2025)" training ...

AdvaMed wants to work with the Trump administration "to recognize and to reward the unique strength of the U.S. medtech ...

FDA clearance is a vital milestone for ASX medical device companies, opening access to the US market while navigating the regulatory process.

South Korea’s medical device market is rapidly expanding, driven by technological innovations and increasing healthcare demands. As the market grows, understanding Korean medical device regulations is ...

In the intricate and highly specialized domain of medical device regulatory affairs, successful navigation demands rare expertise that harmonizes scientific rigor with regulatory precision, ultimately ...

The Elena and Miles Zaremski Law Medicine Forum presents: Medical Device Regulation: Going from Bad to Worse...or Better? with George Horvath Innovations in medical device technology hold the ...

Despite the fresh set of guidelines, experts said that technologies like AI are increasingly being used in MedTech sector, ...

Draft guidelines aim to align India's medtech software framework with global practices; industry seeks more clarity on AI/ML ...

As the biopharma space gets more competitive and the days of blockbuster drugs seem further in the rearview, biopharma companies are investing in digital to find new and innovative ways to ...