Services
As a service provider for researchers in the public and private sectors, we have been providing a wide range of services to our clients for more than 10 years. We submit existing study protocols to the relevant ethics committees and monitor clinical trials as part of quality assurance.
Our staff have more than 20 years of experience in the submission of multicentre studies, thus ensuring that even complex, multicentre studies can be successfully submitted and launched.
The monitoring of clinical studies is absolutely necessary for quality assurance and a prerequisite for the validity of the study data. Study monitoring usually takes place on site. Our staff are experienced in the domestic market, as well as European and non-European countries.
What we offer
We offer a range of services including the following:
- Study submission
- Submission of studies to the relevant ethics committees and regulatory authorities.
- Monitoring
- Monitoring of clinical trials in accordance with current guidelines (including GCP).
- Reporting
- Preparation and forwarding of the necessary progress reports to ethics committees and regulatory authorities.
- Support
- We support researchers in the preparation of final reports, study protocols and other documents.
- Training
- We train researchers in the correct implementation of study protocols.