News & Events

Tips to Design a High-Quality PMCF User Survey

With the implementation of the Medical Device Regulation (2017/745) (MDR) in the EU, post-market clinical [...]

Free Webinar – Tips and Tricks on How to Get Started with a Clinical Study under MDR

Date: 8 December, 2022Time: 16:00 – 16:45 CEST | 10:00 AM – 10:45 AM EST [...]

State of the Art: What does it Mean in Practice?

More and more focus has been given to the state of the art in the [...]

Jelena Kresoja joins Qserve

Jelena Kresoja has joined Qserve Group as a medical writer for PMCF, where she is [...]

Team-NB Position Paper

This position paper includes a definition of ‘systemic off-label use’ (device used repeatedly or continuously outside [...]

Meet our team at the 4th Annual European Conference on Proactive Surveillance and Post-Market Vigilance of Medical Devices

Date: 4 and 5 October 2022Emplacement: Brussels, BelgiumLanguage: French/English Qserve CRO is pleased to be attending the 4th [...]

Iris Verboven returns to Qserve CRO

We are pleased that Iris Verboven returned to Qserve CRO to strengthen the clinical team [...]

Laura Castro joins Qserve

We are pleased to announce that Laura Castro joined the Qserve Group, where she is [...]

Clinical Evaluation and Sufficient Clinical Evidence

Clinical Evaluation requirements have increased dramatically. The process now involves three documents: the Clinical Development [...]

Bianca Lutters PhD – Head of Qserve Clinical Operations including CRO

Qserve CRO is proud to announce new leadership within the Clinical Division effective September 1st.  [...]