Dublin, Sept. 24, 2025 (GLOBE NEWSWIRE) -- The "A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU (European Union) and UK Training Course (Oct 21, 2025)" training ...
DUBLIN--(BUSINESS WIRE)--The "The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation) Training Course" ...
The evolving EU MDR and IVDR present key opportunities for companies to enhance compliance strategies, engage with notified bodies, and optimize market access. Staying informed and proactively ...
It wasn’t so long ago that many of us mocked the validity of an online education. Often this form of higher learning was dismissed as merely ‘mail order degrees’ that inferred an almost tabloid ...
In February 2026, the medical device industry will be faced with new regulatory challenges that could shake up operations. The good news? Companies that are already in compliance with existing FDA ...
The "FDA Regulatory Compliance for Drug and Biotech Products (Nov 12th - Nov 13th, 2025)" training has been added to ResearchAndMarkets.com's offering. Regulatory Compliance is the level of activity ...
Software is increasingly used as a medical device, transforming the healthcare industry with the goal of improving patient outcomes. However, developing software as a medical device involves ...
The "An Introduction to the Medical Device Regulation Training Course" conference has been added to ResearchAndMarkets.com's offering. This seminar provides an invaluable overview of the European ...
Artificial intelligence (AI) in health care is rapidly advancing beyond traditional applications. Autonomous AI agents are gaining significant attention for their potential to fundamentally transform ...
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