Clinical Trials and Pharmacovigilance

Attendees will explore innovations in clinical trial designs, including adaptive trials, real-world evidence, and patient-centric models. Sessions will also address pharmacovigilance and drug safety, highlighting post-market surveillance, adverse event reporting, and risk management strategies. The integration of technology, such as electronic data capture (EDC) systems and AI-driven analytics, has transformed both fields. Adaptive trial designs and real-world evidence collection enhance efficiency and relevance, while advanced pharmacovigilance tools predict and identify potential risks earlier.

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