Post-Market Surveillance (PMS)
What is Post-Market Surveillance (PMS)? Post-Market Surveillance (PMS) refers to the continuous monitoring and evaluation of pharmaceutical products, medical devices, or APIs after they have been released into the market. It involves systematically collecting, analyzing, and interpreting data on product performance, adverse effects, and safety signals to ensure ongoing compliance with Good Pharmacovigilance Practices (GVP) and regulatory standards. PMS is a […]
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