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Clinical investigations with medical devices (MDR)
Standard research file medical devices
K. Other documents
Search within English part of The Central Committee on Research Involving Human Subjects
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K. Other documents
This part of the file contains other documents relevant to the clinical investigation.
K1. Recommendations other authorities
K2. Assessment other EU member states
K3. Clinical trial agreements
K4. Scientific publications
K5. Data Safety Monitoring Board (DSMB)
K6. Other information
K7. Clinical Evaluation Plan
K8. Description of the processing of personal data
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