News & Events

Outsourcing In Clinical Trials: Medical Devices Europe 2023

Date: 21-22 February, 2023Location: Holiday Inn Munich City Centre, Munich, Germany Introduction The 2023 programme [...]

Marloes van der Hagen joins Qserve

We are pleased to announce that Marloes van der Hagen joined Qserve Group as a [...]

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 [...]