Post Marketing Clinical Follow-up (PMCF) is a vital phase in the life cycle of medical devices and pharmaceutical products. It involves the collection of real-world data after a product has been authorized for market use, allowing for continued assessment of safety and efficacy in diverse patient populations. PMCF studies provide valuable insights into the long-term systematic monitoring and evaluation, PMCF contributes to the refinement of medical interventions, fostering continuous improvement in healthcare outcomes performance and potential risks associated with the product, helping to ensure ongoing patient safety and regulatory compliance.

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