Clinical Monitoring & Site management

Quality of clinical monitoring is pivotal in the success of each clinical trial. Our highly educated and trained monitoring professionals conduct clinical monitoring activities under ICH/GCP standards, they adhere to FDA/EMEA regulations and to our or our clients’ SOPs. All KCR CRAs located across Europe are fluent in local languages and work while maintaining a unique professional interaction with PI’s and site’s personnel.

KCR is constantly trying to be proactive while interacting with research teams.  This strategy has helped us to build strong and positive relationships with our investigators. 

Additionally, KCR cooperates with an expansive network of outpatient clinics and private hospitals in Poland whom have access to large databases containing thousands of patients.