MD+DI has compiled a list of the most influential companies in the market. Omar Ford is a veteran reporter in the field of medical technology and healthcare journalism. As Editor-in-Chief of MD+DI ...

IVDs are defined in the new EU IVDR legislation as: “Any medical device ... CE mark for medical devices and IVDs until 2028 and 2030, respectively, at which point manufacturers will be required ...

MedTech Europe’s report reflects a lack of clarity over requirements, rising costs, and decreases in innovation activities.

Among the wave of guidance documents issued by the U.S. Food and Drug Administration (“FDA” or the “Agency”) in the first week of 2025 were ...

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 ...

The National Capital Consortium for Pediatric Device Innovation (NCC-PDI) announces eight winners chosen in its special COVID-19 edition of the “Make Your Medical Device Pitch ... the Johnson & ...

The MHRA has issued fresh guidance to help medical device manufacturers prepare for upcoming regulatory changes.

Ministry of Chemicals and Fertilizers data shows India's export growth in medical implants and consumables, highlighting ...

To prevent misuse of raw materials collected from blood centres, the Union health ministry has issued new norms for domestic manufacturers ... (IVD) reagents. Also Read | Medical devices maker ...

The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a suite of guidance specifically designed to help medical ...