Pharmacovigilance and ADRs Reporting

Pharmacovigilance plays a critical role in ensuring the safety and efficacy of pharmaceutical products throughout their lifecycle, including clinical trials.

Integrating pharmacovigilance practices into clinical operations is essential for identifying, assessing, and managing adverse events and other safety-related information in real-time.

Our pharmacovigilance team monitors adverse events and safety data throughout the trial, promptly reporting any safety concerns to regulatory authorities and study sponsors.