Services
Clinical trials
We have a comprehensive offer in the field of planning, organization and monitoring of clinical trials. We are involved in both commercial and non-commercial projects (e.g. implemented as part of subsidies and grants)
Clinical
Opinion on the assumptions of clinical trials
Assistance in the preparation of audit documentation required by law
Reporting and an account on the progress of the study
Coordination of clinical trials in problematic centers
Managing the process of monitoring clinical trials
CRA delegation under employee leasing
Contracting and setting up test systems (e.g. eCRF, IWRS)
Organization of the “Start-up” phase of the study (selection and contracting of sites; preparation of submissions to the Bioethics Committee and URPL)
Services
Observational Studies
We have a comprehensive offer in the field of planning, organization and monitoring of observational (non-interventional) studies.
Help in publishing the results
Ongoing supervision over the observational study and coordination of the data collection process
Assessment of the project in the context of the feasibility of an observational study, rather than a clinical study
