Free Webinar – Clinical Submission Strategy Europe and United Kingdom
Date: 15 February, 2023 Time: 17:00 – 18:00 PM CEST | 11:00 AM – 12:00 [...]
Dec
Webinaire gratuit 8 dec 2022
Conseils et astuces pour démarrer une étude clinique dans le cadre du RDM 2017/745 Agenda [...]
Nov
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 [...]
Nov
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 [...]
Nov
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 [...]
Oct
Jelena Kresoja joins Qserve
Jelena Kresoja has joined Qserve Group as a medical writer for PMCF, where she is [...]
Oct
Team-NB Position Paper
This position paper includes a definition of ‘systemic off-label use’ (device used repeatedly or continuously outside [...]
Oct
Meet our team at the 4th Annual European Conference on Proactive Surveillance and Post-Market Vigilance of Medical Devices
Date: 4 and 5 October 2022 Emplacement: Brussels, Belgium Language: French/English Qserve CRO is pleased to be attending [...]
Sep
Iris Verboven returns to Qserve CRO
We are pleased that Iris Verboven returned to Qserve CRO to strengthen the clinical team [...]
Sep
Laura Castro joins Qserve
We are pleased to announce that Laura Castro joined the Qserve Group, where she is [...]
Sep