Monatliche Archive: März 2020

Health authority responses to the COVID-19 impact on clinical research

The COVID-19 crisis places a huge burden on the healthcare systems of countries around the [...]

Fifteen most-frequently asked questions on Clinical Evaluation for Europe

One of the significant changes in EU regulatory science for medical devices is the enhanced [...]

Webinar: What you should know when designing a PMCF Plan for your Medical Device

According to the KPMG/RAPS survey results published in September 2019, 43% of Medical Device respondents [...]

Meet and Greet with Wiebe Postma at the 4th Annual European Medical Device Investigator Initiated Study Meeting

January 29, 2020 – January 30, 2020 / Europe – Brussels, Belgium (Sheraton Brussels Airport Hotel, Belgium) [...]

Monitoring in Medical Device studies: what is needed?

If you are a manufacturer who started a clinical trial, then you have the obligation [...]

The research naïve study site – always a problem?

Your potential investigator / KOL is very enthusiastic to do your study but does not [...]

Introduction to our Qserve CRO website by Loes Pelgrim

We understand the challenges, we see opportunities and will find the solutions. Learn more about [...]

Key Opinion leader engagement for your clinical investigation

What can KOLs add to your Clinical Investigation? Key opinion leaders (KOLs) are experts and [...]

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