CRS is a CRO with 275 clinical pharmacological beds. All of the CRS CPUs are located in metropolitan areas (Kiel, Berlin, Wuppertal, Mönchengladbach & Mannheim) in Germany to ensure fast recruitment of patients, symptom bearing or healthy volunteers in order to conduct large scale and long-lasting clinical trials.
The service panel of CRS in phase I-II human pharmacological trials includes BE/BA, FIM, POC, patient trials and specialties like QTc and renal/hepatic insufficiency. The in-house modular services Consultancy, Clinical Data Management (CDM), Statistical Analysis (STAT), Medical Writing and Clinical Trial Supply Management (CTSM) support the clinical conduct according to the client’s individual needs.
Over the past decades, the group has performed several hundreds of clinical trials, maintaining rigorous adherence to GCP-guidelines to attain the highest quality. Besides GCP, all activities are running in accordance with the respective GxP standards. This high quality has been confirmed several times by local, national and international authorities.