Archives: News

As healthcare professional or institute – what does the new medical device regulation change for you?

How to determine what Post Market Clinical Follow-up activities to initiate?

Case Story – Investigator Initiated Studies

Are you our new CRA?

The new Medical Device Regulation – and its impact on innovation

Are your investigator and site ready for an FDA inspection? – Part 2

Are your sites prepared for FDA inspection of your clinical investigations in EU?

MEDDEV 2.7/1 Rev 4 Clinical Evaluation: Are you ready to update your clinical evaluation report.