Mission:
Clinical Trial Service B.V. as a Contract Research Organization contributes to the optimization process of qualitatively high and reliable clinical research by transferring knowledge and experience obtained by setting up, monitoring and managing clinical research: drugs, medical devices and food supplements.
Knowledge and experience are transferred to research centres during initiation visits and the monitoring of clinical trials, but definitely also during the specially developed ICH-GCP training for research staff, medical specialists and general practitioners.
By implementing the product SOPs for Sites, Standard Operating Procedures clinical trials for research centres CTS tries to improve the quality of research performed in the research centres. So research centres are able to conduct clinical trials according to the most recent (inter)national guidelines for clinical research ánd according to the high quality requirements requested by sponsors.