Transcription of Technical Documentation Requirements under MDR
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Technical Documentation Requirements under MDR
1 Technical Documentation Requirements under MDR (including Requirements for legacy files) Dr Amie Smirthwaite Clinical Oversight and Training Lead BSI Notified Body 2 Topics Overview of Technical Documentation Requirements New Requirements ? Clinical investigations and equivalence Reclassifications 3 Overview of Technical Documentation Requirements 4 MDR Requirements for Technical Documentation 1: Device description 2: Information to be supplied by the manufacturer 3: Design and manufacturing information 4: General safety and performance Requirements 6: Product verification and validation 5: Benefit-risk analysis and risk management Annex II: Technical Documentation 5 MDR Requirements for Technical Documentation 1: Device description 2: Information to be supplied by the manufacturer 3: Design and manufacturing information 4: General safety and performance Requirements 6: Product verification and validation 5: Benefit-risk analysis and risk management Annex II: Technical Documentation Annex III.
tooth crowns, screws, wedges, plates, wires, pins, clips or connectors •Equivalent devices must have sufficient clinical data •PMCF studies should be in place •devices must have sufficient clinical data •Compliant with CS if available
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