Catania, Italy, December 12th, 2025, FinanceWireNTA Implant (Pilatus Swiss Dental GmbH), the Swiss-origin, MDR-certified ...

On November 8, 2025, the Department of Health published proposed amendments to the Medical Devices Regulations, SOR/98-282 ...

Navigating the SaMD regulatory pathways is one of the most complex yet important aspects of product development for medical technology startups. Startups in this field are required to meet local ...

Galderma opens up new chapter for Sculptra with MDR certification and new expanded indication for body: Zug, Switzerland Monday, December 8, 2025, 12:00 Hrs [IST] Galderma, the pu ...

Qase3D introduces MDR system form hospital 3D labs - a practical, legally grounded path to MDR compliance for Point-of-Care ...

CDSCO launches new online risk classification module for medical devices to simplify approval procedures: Gireesh Babu, New Delhi Tuesday, December 9, 2025, 08:00 Hrs [IST] The Ce ...

On 27 November 2025, Commission Decision (EU) 2025/2371 of 26 November 2025 declaring the functionality of the first four EUDAMED modules ...

Remote monitoring has become an essential component of virtual wards and community-based care. As adoption accelerates, understanding medical-device classification is not a legal technicality, but a ...

St. Paul medical device companies Minnetronix Medical and Intricon recently merged to form a new contract design and ...

Lawmakers requested the report after a 2023 ProPublica and Pittsburgh Post-Gazette investigation revealed that the FDA had ...

In today’s cosmetic industry, scientific validation has become the foundation of product credibility. Consumers no longer ...

Elon Musk's brain implant company Neuralink has tapped a top U.S. health regulator responsible for overseeing the company and ...