Pharmacovigilance involves monitoring of ADR. In this the adverse effects of the drug are noted and the data is sent to the ADR Monitoring Centres about the case. If any life threatening disease or disability occured to the vounteer then compensation is provided.
We make sure to follow the process as per GCP guidelines, and reports ADR keeping our Executive at the site when the trial is in place keeping the process real time, and transparent to the sponsor.

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