GCP Training for Investigators and Study Nurses / Study Coordinators

For many years the Contract Research Organization proinnovera has successfully been conducting clinical trials. Based on our experience in this field we have also been offering GCP-training since 2008.

The advanced training courses take place in Muenster on a regular basis four to five times a year. Upon request our experienced instructors also train you and your team on a spot at your investigational site or during investigator meetings.
 
Within the GCP trainings the investigator tasks and responsibilities according to ICH-GCP guideline and legal requirements will be discussed. The training program covers alls topics of relevance for a high-quality conduct.
 
According to legal requirements meanwhile implemented by the Ethics Committees, physicians who want to participate in the conduct of clinical trials need proof of GCP training. At the end of our GCP training you will receive a certificate of attendance which can be submitted to the responsible Ethics Committees as evidence of your qualification as clinical trial investigator.
 
Our GCP trainings so far have been certified within the medical education system by Westphalia-Lippe Medical Council (Ärztekammer Westfalen-Lippe).
 
Each medical attendee will presumable obtain nine medical education points.
 

Glossar