The clinical monitor or CRA (Clinical Research Associate) is the link between Sponsor/CRO and the Investigational Site. In response to the increasing and diverse requirements and demands, the CRA's role has changed considerably over the past years, evolving from controller to a competent site manager.
Based on our longstanding experience we realise and serve the needs of sponsors and investigators/ investigator's staff. We combine good quality control at the investigational site with individual, supportive measures and excellent communication.
Our CRAs are experienced in both, quality control and contact with investigators and their staff. On the basis of the monitoring manual, our CRAs supervise and support the clinical trial conduct "on site" and/or by using digital technologies ("remote").
Use our experienced monitors for the supervision and the support of your investigational sites and for quality control!