Category Archives: Blog
Celien van Lochem has joined Qserve
We are pleased to announce that Celien van Lochem has joined Qserve as a business [...]
Dec
A message from our CEO
Our CEO Jan van Lochem will give you an update on the current market status [...]
Aug
The new ISO 14155 standard for Good Clinical Practice is now published!
After many delays it is now officially available: the new ISO14155 standard for clinical investigations [...]
Aug
What are side-effects and what is their relationship to residual risk and adverse events?
We are all familiar with the listings of side-effects in the package insert of medicines [...]
Aug
Investigator Initiated Studies, what are they and how can they be of value to your company?
Investigator Initiated Studies (IIS) are clinical investigations that are started by physicians. As opposed to [...]
Jul
Clinical data collection during a pandemic; not an impossible task
How to avoid delay and non-compliance of your PMCF activities With full MDR implementation less [...]
Jun
How PMCF surveys can help collect clinical evidence remotely during the COVID-19 pandemic
Due to the COVID-19 pandemic many clinical investigations other than those aimed at management of [...]
May
3 reasons why you should use a medical device dedicated CRO
Wiebe Postma shares three reasons with you about why you should use a medical device [...]
Apr
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 [...]
Mar