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Clinical investigations with medical devices (MDR)
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K. Other documents
This part of the file contains other documents relevant to the clinical investigation.
K1. Assessments other institutions
K2. Assessment other EU member states
K3. Clinical trial agreements
K4. Scientific publications
K5. Data Safety Monitoring Board (DSMB)
K6. Other information
K7a. Clinical Evaluation Plan
K8. Description of the processing of personal data
