Information for volunteers and patients in our clinical studies.
A clinical trial is a scientific study involving human subjects to evaluate drug efficacy and safety. Participation is always voluntary and requires written informed consent.
Depending on the study, we recruit healthy volunteers (for bioequivalence studies) and patients with specific conditions (for Phase II-IV trials). Every candidate receives a free medical evaluation.
All studies are approved by an independent Ethics Committee and conducted per ICH GCP E6(R2) international standards. Participant health and safety is our top priority.