The "A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU (European Union) and UK Training Course (Apr 29, 2026)" training has been added to ResearchAndMarkets.com's ...

Boston Scientific agreed to buy medtech firm Penumbra in a $14.5  billion deal on Thursday, its second‑largest takeover ever, ...

Soon after the FDA’s guidance release, two other major AI announcements also hit the news: Utah began a first-in-the-nation pilot with Doctronic for autonomous AI prescription refills, and OpenAI ...

The EU's IVDR provides a regulatory basis for establishing the safety and effectiveness of new in-vitro diagnostic (IVD) ...

Within the category of In Vitro Diagnostic (IVD) devices, IVD consumables are projected to experience the highest compound ...

DNV is a trusted Notified Body for medical device certification under the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). We provide independent, rigorous, and ...

At its J.P. Morgan Conference 2026 presentation, Qiagen NV alluded to positive full-year results for 2025 and expressed that ...

DNV, the independent global assurance and risk management provider, is partnering with Korean AI-driven blood and cancer ...

Great Britain is entering a new era of MedTech regulation, with major pre-market changes expected that are designed to ...

New options for testing and treating some of the most common sexually transmitted diseases are becoming available ...

Biocartis to collaborate with Mayo Clinic on breast cancer gene signatures ...

Abstract: While noninvasive medical devices for disease diagnosis and management are used routinely in high-income settings, their penetration in low-income countries, and in complex emergency and ...