What looked like a simple key chain turned out to be an initiator. While it wasn't active, it was still a prohibited item.

It is barely the second quarter of the year, yet the Kenyan healthcare regulatory landscape is being redrawn. Two documents released in 2026 will be major determinants of how pharmacies, clinics, ...

BOSTON--(BUSINESS WIRE)--InterSystems, a creative data technology provider powering more than one billion health records globally, today announced that its electronic health record (EHR) solutions ...

Regulatory milestone reaffirms InterSystems as a leading provider of enterprise-grade AI applications InterSystems, a creative data technology provider powering more than one billion health records ...

The European Commission on Tuesday published an implementing regulation that outlines uniform quality management and procedural requirements for conformity assessment activities conducted by notified ...

Psychological stress plays a critical role in shaping performance and well-being in competitive sport. This mini-review examines three major categories of psychological interventions for stress ...

The European Commission’s Medical Device Coordinating Group (MDCG) has revised several documents addressing the classification of products under the Medical Device Regulation (MDR) and the In Vitro ...

FDA has moved artificial intelligence (AI) in medical devices from an exploratory concept to operational expectations, finalizing a pathway to pre-approved algorithm updates (PCCPs), publishing ...

Device Makers are currently at an intersection of accelerated innovation and heightened regulatory scrutiny. Regulatory affairs stands in the center guiding operational resilience and a coherent ...

Jan 6 (Reuters) - The U.S. Food and Drug Administration said on Tuesday that it will limit regulation of wearable devices and software designed to support healthy lifestyles, issuing new guidance to ...