Post-market surveillance for devices and IVDs: a f...

The entry into force of the Regulation (EU) 2017/745 on devices  medical

Evamed showcases comprehensive clinical support for medical device manufacturers at EUCROF24
Evamed showcases comprehensive clinical support fo...

Evamed, a leading French clinical research company specialising in the evaluation and

1MED Unveils Ground-breaking Solutions to Navigate...

1MED a specialist Contract Research Organisation (“CRO”) providing clinical and regulatory support

1MED’s New Partnership with Accenture!

We are thrilled to announce a game-changing collaboration between 1MED, a leading

Discovery Pack – MDD to MDR

MDR Grace Period ends May 26th 2024. As this date approaches, manufacturers

An insight on the improvements in the medical devi...

From today we start the distribution of our video in the US

TOP 5 most urgent tasks for MDR compliance before ...

Following the success of the 1TALK event on November 30th, 1MED team

DISPOSITIVI MEDICI E DATI CLINICI – focus su...

1MED ha proposto il webinar 1TALK  “Dispositivi medici e dati clinici, focus sui

1MED and Apposite Capital partner to support excel...

Apposite Capital, the healthcare specialist private equity investor, today announces that it

Generation of compliant, pre-clinical, biocompatib...

The approach to biological evaluation for medical devices has significantly changed in