The "Medical Device Regulatory Affairs Market Size, Share & Trends Analysis Report By Type, By Service Provider, By Service, ...

For those with Class IIa or above AI-related devices, compliance with the EU’s AI Act is likely to be akin to the EU MDR.

Market Surveillance - Practical Application for Medical Devices and IVDs Training Course (ONLINE EVENT: February 12, 2025)" has been added to ResearchAndMarkets.com's offering. Understanding the ...

As medical devices become more complex, and as regulatory requirements become more rigorous, it’s imperative that medical devices using electronic components are developed as efficiently as possible.

In 2024, as in years past, healthcare fraud enforcement by the U.S. Department of Justice (DOJ) was substantial. Federal actions under the ...

This piece is part of a series that dives deeper into the most prevalent themes of this year’s iteration of our flagship research piece, Charting Disruption. Click to read.

The US Food and Drug Administration (FDA) recently issued its draft guidance, Considerations for the Use of Artificial Intelligence to ...

The Union Budget 2025, the second full budget of Modi 3.0 may bring a variety of changes such as income tax reforms, an ...

In digital healthcare, AI drives innovations and improves patient outcomes by making processes more efficient.

NXP recently launched the EdgeLock A30 Secure Authenticator chip, a Common Criteria EAL 6+ certified secure authentication ...

Dou Yee's Role as a Reseller As part of its new role as a reseller for BIOVIA solution in Southeast Asia, Dou Yee Enterprises ...