USA | FDA Publishes Final Guidance for Medical Device Postmarket Surveillance (522 Order)
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GERMANY | BfArM Tightens Data Protection Requirements for DiGAs
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AUSTRIA | New NIS Classification Guidelines for Medical Devices
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EU | Notice to Manufacturers to Ensure Timely Compliance with MDR Requirements
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UK | NICE’s New Early Value Assessment for Medtech
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FINLAND | New Article 82 MDR Regulation
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China | CMD Publishes 2022 China NMPA (CFDA) Blue Book: Revised Medical Device and IVD Regulation
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USA – Real-World Evidence Landscape Review: Insights on the Use of RWE from Stakeholders Across the Medical Device Ecosystem
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USA – Independent assessment of the NESTcc Test-Cases: RAND Interim Report Provides Insights from RWE Generation for Medical Devices
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