Study processes

In addition to the complete conduct of clinical trials and non-interventional studies (NIS), we offer competent support in the following sub-processes:

Study Management

Data Management

Monitoring

Statistics

Medical Writing

Regulatory Affairs

Drug Safety

In addition to our broad know-how benefit from our flexible contract options, e.g. service / work contracts and contracts according the Temporary Employment Act. We are available as a long-term service provider and also support you flexibly in times of shortages.

Our experts will gladly advice you personally. We look forward to your call or your message.