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Pharmacovigilance is the science of monitoring, assessing, and preventing adverse effects associated with medical products. In clinical research, it plays a critical role in ensuring patient safety throughout the study lifecycle. Adverse events are carefully recorded and analyzed to identify potential safety risks. Serious and unexpected reactions are reported promptly to regulatory authorities. Pharmacovigilance activities continue even after a product is approved, ensuring long-term safety in real-world use. This ongoing surveillance helps refine treatment guidelines and improve patient care. By integrating pharmacovigilance into clinical research, organizations maintain safety, compliance, and public trust. https://clinicalresearchdental.blogspot.com/2025/11/the-role-of-clinical-research-in.html https://clinicalresearchdental.blogspot.com/2025/11/how-clinical-research-is-creating-new.html https://ptechnobridge.wordpress.com/2025/11/25/clinical-research-a-promising-path-in-modern-healthcare/ https://ptechnobridge.wordpress.com/2025/11/25/the-expanding-landscape-of-clinical-research-and-its-growing-career-scope/ https://ptechnobridge.wordpress.com/2025/11/25/the-role-of-clinical-research-in-building-safer-and-smarter-healthcare-systems/ https://ptechnobridge.wordpress.com/2025/11/25/how-clinical-research-is-creating-new-opportunities-for-future-professionals/ https://patrickbridge.substack.com/p/clinical-research-a-promising-path https://patrickbridge.substack.com/p/the-expanding-landscape-of-clinical https://patrickbridge.substack.com/p/the-role-of-clinical-research-in https://patrickbridge.substack.com/p/how-clinical-research-is-creating
