QualityCR is an independent consultancy company based in the Netherlands and serves the research oriented pharmaceutical industry as well as academia.

We offer independent Quality Assurance and Risk Management consultancy focusing on the quality management in clinical research. Moreover, we offer tailored trainings in GCP and quality management.

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Auditing helps providing insight into the quality of your clinical research


We help you prepare for audits and how to manage clinical research with a risk-based approach

Continuous training is essential to maintain the best performance of your personnel


We organize trainings - like Good Clinical Practice - to help you maintain the best performance of your personnel



Take a look at our portfolio to learn more about our partners. 

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Read the full news articles about our company and branche news.

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EMA publishes new Trial Master File (TMF) guideline for consultation

17-04-2017 / Daniela / Branche

The European Medicines Agency (EMA) has published on 12/04/2017 the draft version of new guideline “on good clinical practice compliance in relation to trial master files” (TMF). This document includes…

External guidance on the implementation of the European Medicines Agency policy on the publication of clinical data for medicinal products for human use

17-04-2017 / Daniela / Legislation

The document below provides guidance on practical aspects of the implementation of the Agency's policy on the publication of clinical data for medicinal products for human use.

It covers guidance regarding:

- procedural aspects…