News & Events

Amber Majoor joins Qserve

We are pleased to announce that Amber Majoor joined Qserve CRO, where she is part [...]

A New ISO 18969

A New ISO 18969 – “Clinical Evaluation of Medical Devices” Is on the Way: Understanding [...]

Free Webinar – Clinical Decision Software – What does is practically mean?

Date: 20 December, 2022Time: 17:00 – 18:00 PM CEST | 11:00 AM – 12:00 PM [...]

Free Webinar – Clinical Submission Strategy Europe and United Kingdom

Date: 15 February, 2023Time: 17:00 – 18:00 PM CEST | 11:00 AM – 12:00 PM [...]

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 [...]

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

Language: English Agenda This webinar will give insight into preparing for and initiating a pre-CE clinical [...]

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 [...]

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