The Three Pillars of Clinical Evidence Under the IVDR
The IVDR raises the bar. Many in vitro diagnostic (IVD) medical device manufacturers still ...
Prepare your clinical study for success
Many innovative therapies and medical technologies face the same challenge: you know a clinical ...
The IVDR transition is not over: key deadlines and common pitfalls
The core shift, as a reminder. IVDR (EU) 2017/746 replaced the former IVD Directive's largely ...
Medtechdagen: 24 September
This year Medtechdagen (Medtech Day) will be held on 24 September in Stockholm, Sweden. ...
IEC 62366 Medical device usability course: 07 October
This 1-day course on IEC 62366 Medical Device Usability, in collaboration with Intertek Academy, is ...
Medtech Compliance Forum: Scientific programme now available
The Medtech Compliance Forum by Aurevia & RAPS is a dedicated platform within Labquality Days, ...
COG CRO Summit Europe: 15-16 September
We hope to see you at the COG CRO Summit Europe in Amsterdam. We will be joining CRO leaders and ...
Need support with EUDAMED?
EUDAMED registration is now an important part of regulatory compliance for medical device and IVD ...
Do you know your bridges?
This bridge is more than a landmark. It's also part of a fun challenge waiting for you at the ...