Clinical Trial and Bioequivalence Monitoring

We are the quality partners emerged to assure that, the clinical trial or bioequivalence study has been conducted in accordance with the protocol, regulatory guidance, SOPs. Will ensure the objective, purpose, integrity of the trial, safety and wellbeing of study participants are protected. Our Monitoring service scattered across nonclinical and clinical phases of the product development. Our Monitoring strategy is well planned to meet the requirements of the sponsor and regulatory authorities across the globe. We have dedicated Clinical, Laboratory, Medical monitors for each study sponsor separately and every Monitor will train on protocol before reaching and initiation of the study at site. All Monitors will work in synergy with central monitoring team for addressing the feasibility and real time challenges. Our Monitors have extensive experience in various therapeutic areas of health sciences