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 ...

Cambridge, UK - Regulatory compliance in medical device development is often treated as a hurdle to be cleared late in a ...

These definitions as written out by AAMI (The Association for the Advancement of Medical Instrumentation) offer clarity, helping designers recognize and address these risks effectively in product ...

As part of its efforts to regulate the medical devices in the country, the Drugs Controller General (India) has issued a notice classifying 77 medical devices pertaining to oncology under the ...

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 ...

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 ...

The prediction that healthcare data would be aggressively targeted by ransomware attacks in 2017 has proven to be true. The malicious WannaCry ransomware attack spread to over 150 countries and ...