『EU MDR Clinical Investigations: Navigating Deadlines and Data Requirements for European Market Access』のカバーアート

EU MDR Clinical Investigations: Navigating Deadlines and Data Requirements for European Market Access

EU MDR Clinical Investigations: Navigating Deadlines and Data Requirements for European Market Access

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 This episode provides a detailed overview of the clinical investigation requirements under the European Union's Medical Device Regulation (MDR). We explore the critical distinctions between pre-market clinical investigations and post-market clinical follow-up (PMCF), the role of the Clinical Evaluation Report (CER) as a living document, and the key transitional deadlines that manufacturers of legacy devices must meet to maintain market access. We also touch on the function of the EUDAMED database in enhancing transparency. - What are the primary differences between clinical data requirements under the old MDD and the current MDR? - How does the MDR define a pre-market clinical investigation versus a post-market clinical follow-up (PMCF) study? - What were the critical compliance actions required by the May 26, 2024, deadline for legacy devices? - What is the significance of the September 26, 2024, deadline for agreements with Notified Bodies? - Why is the Clinical Evaluation Report (CER) now considered a living document that requires continuous updates? - What are the final transition deadlines for different device risk classes to become fully MDR compliant? - How will the EUDAMED database impact the transparency of clinical investigations in the EU? - What are the general requirements for reporting serious adverse events during a clinical investigation under the MDR? Navigating the EU MDR's stringent clinical evidence requirements demands deep regulatory expertise. Pure Global provides end-to-end consulting for MedTech and IVD companies, leveraging local experts and advanced AI to streamline global market access. We develop efficient regulatory strategies, use AI to compile technical dossiers, and act as your local representative to ensure you meet all pre-market and post-market obligations. To learn how we can accelerate your entry into over 30 global markets, visit us at https://pureglobal.com/, contact info@pureglobal.com, or explore our FREE AI tools and database at https://pureglobal.ai.
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