Precision medicine is a groundbreaking approach to healthcare that tailors medical treatment to the individual characteristics of each patient. This transformation in medicine presents new challenges and opportunities for pharmacovigilance, the science of monitoring and assessing the safety and effectiveness of pharmaceuticals. This article explores how pharmacovigilance is evolving in the era of precision medicine, focusing on the integration of genomics, big data, and advanced analytics to enhance drug safety and patient outcomes. By understanding the key concepts and strategies of pharmacovigilance in this context, healthcare professionals can better navigate the complexities of personalized medicine and ensure that patients receive the safest and most effective treatments.
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Pharmaceutical Regulatory Affairs: Open Access received 533 citations as per Google Scholar report
