In a move aimed at protecting patients as artificial intelligence increasingly enters healthcare, govt has brought AI-based ...

DCGI releases classification of 77 medical devices related to oncology: Gireesh Babu, New Delhi Wednesday, January 7, 2026, 08:00 Hrs [IST] As part of its efforts to regulate the ...

In a significant move aimed at strengthening regulatory clarity for cancer related medical technologies, the Central Drugs ...

ServiceNow, the AI control tower for business reinvention, today entered into an agreement to acquire Armis for $7.75 billion in cash.

Version 4 of the Manual on Borderline and Classification for Medical Devices was published in September by the European Commission’s Medical Device Coordination Group. Our Life Sciences Regulatory ...

1 INVAMED Medical Innovation Institute, New York, NY, United States 2 Med-International UK Health Agency Ltd., Leicestershire, United Kingdom Abdominal and thoracic aortic repairs increasingly rely on ...

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 ...

Medtech pros know there are some things you just can’t find with a Google search or by asking ChatGPT. Sure, those generative AI responses sound confident. But anyone who has queried a large language ...

The U.S. FDA issued a pair of final guidances this week, including one that outlines the criteria for authorizing emergency use of unapproved in vitro diagnostic tests during future public health ...

Medical device design and development is a process that helps to ensure devices that go to market are safe, effective, marketable, and profitable. The process is a blueprint of the phases needed to ...