Master the Art of IVDR Compliance with Our Online Postgraduate Course! Need to navigate the complexities of the In Vitro Diagnostic Devices Regulation? This is your chance to gain the expertise needed to construct a Technical File and Performance Evaluation Report - two essential elements for regulatory compliance. Module 3: Generating Data for Technical Documentation…
MDR/IVDR Implementation and Resource Allocation for C-level Management of MOs is a specialized short course designed for C-level executives. It offers practical training on how to effectively allocate time, budget, and other essential resources needed by Market Operators to prepare comprehensive dossiers for Notified Bodies. 🔹 First step! Create your account on the NoBoCap Environment at https://portal.nobocap.eu.🔹 Then, go to…
Master MDR Compliance with Our Online Postgraduate Course! Need to navigate the complexities of the Medical Device Regulation (EU 2017/745)? This is your chance to gain the expertise needed to construct a Technical File and Clinical Evaluation Report – two critical pillars for regulatory compliance. Module 2: Generating Data for Technical Documentation (MDR) is a…
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