With recent requirements, the FDA is taking a hard stance: cybersecurity is a core consideration with compliance being ...

Venudhar Rao Hajari has built a successful career in the areas of Medical Device Development Quality Assurance, Software ...

Guardpack, a UK-based contract manufacturer of wet wipes and sachets, has secured funding that enables expansion into the ...

ANSI/AAMI ST108:2023 is a new, comprehensive standard for water quality systems in medical device reprocessing.

Europe, comprising 27 EU member states, is one of the world’s largest and most advanced markets, serving over 500 million ...

Expanded Quality Management: Medical devices require rigorous quality management ... In a recent collaboration, an IoT-driven drug-delivery system significantly improved patient outcomes by ...

Neo Medical’s spine care platform fully approved under EU Medical Device Regulation directive: Lausanne, Switzerland Tuesday, December 3, 2024, 12:00 Hrs [IST] Neo Medical SA (N ...

Neo Medical SA (Neo), a Swiss technology company specializing in spine surgery, today announced the approval of its entire product portfolio under the European Union's (EU) Medical Device Regulation ...

Composable software seamlessly integrates with core systems, facilitating communication and real-time data sharing between ...