We offer you the services for organization and conduct of studies. We provide a complete provision of the whole process (the “turnkey study”), and separate the fragments of interest to you, such as:
- Development of the study Protocol
- Preparation of the accompanying documentation (Case Report Form, the researcher’s brochure, informed consent of the patient)
- Selection of a clinical base for the study
- Conduct of monitoring and audit visits to the clinical base
- Organization of the insurance of volunteers participating in the bioequivalence study
- Representation of the interests of your company in the authorized state regulator, etc.
* For getting all proper information, please contact our experts