Focus Area – Compliance for in vitro diagnostic medical devices in the EU
Country – European Union
Related Process – IVD Device Classification, Performance Evaluation and Testing, Regulatory Submission and Approval, Post-market Surveillance, Quality Management System (QMS)
NOTE – Post purchase, you can access your course at this URL – https://mnethhil.elementor.cloud/courses/cr_cs000245-eu-ivdr-in-vitro-diagnostic-medical-device-regulation-compliance-for-european-union/ (copy URL)
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Lessons Included