Connected medical devices can improve patient care and operational efficiency. However, they also introduce new privacy and security risks. Healthcare providers should rethink their privacy and ...

The FDA released their updated guidance on Cybersecurity in medical devices: Quality System Considerations and content for Premarket submissions at the end of June in 2025. In this guidance the FDA ...

Fake ISO certificates claiming safety and quality of medical devices need to be verified: Experts: Shardul Nautiyal, Mumbai Thursday, January 15, 2026, 08:00 Hrs [IST] Experts hav ...

Learn how to develop and obtain market authorisation in the EU for medicinal products, therapies and medical devices intended for human use.

Medical software is the backbone of modern healthcare, supporting electronic health records (EHRs), diagnostic systems, imaging technologies and embedded software in medical devices like pacemakers ...

Regulatory oversight has instead been exercised by the NAFDAC pursuant to its general mandate under the NAFDAC Act (Cap N1, ...