Post Marketing Surveillance

Post-marketing surveillance (PMS) is a critical phase of pharmaceutical regulatory science, focusing on monitoring the safety of medications after they are released on the market. It helps in identifying and evaluating previously unreported adverse effects and interactions, ensuring the ongoing assessment of the risk-benefit balance of drugs. PMS data contribute to updating drug labels, informing healthcare professionals and the public, and may lead to regulatory actions such as modifying dosage recommendations or withdrawing drugs if necessary.

Post-marketing surveillance (PMS) is a vital phase in the lifecycle of pharmaceutical products, aimed at ensuring their ongoing safety once they have entered the market. Through PMS, regulatory authorities and drug manufacturers collect and analyze real-world data on adverse drug reactions, thereby gaining insights into the drug's performance in a broader patient population. This continuous monitoring helps in identifying rare or long-term side effects not detected during the initial clinical trials, ensuring that healthcare professionals and patients are informed about the benefits and risks of medications, leading to safer use of drugs.

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