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Biological evaluation of Medical Devices
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950
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Design of Experiments – DOE
€
250
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GIVIMP and GCCP for scientists
€
950
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GMP for Clinical Trial Material (CTM)
€
490
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ISO13485:2016 – from an auditing perspective
€
950
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IVDR in a nutshell – Risk Management
€
490
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IVDR in a nutshell – Technical Documentation
€
490
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Validation of Analytical Procedures Made Easy
€
250
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CGMP för kvalitetskontroll (QC) och analysarbete
€
620
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Clinical Evaluation for Medical Devices
€
950
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EU GMP Annex 1 – Highlight of the new industry requirements
€
350
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Grundkurs i GMP och kvalitetssystem
€
620
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Introduction to GMP and Quality Systems
€
620
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IVDR in a nutshell – the Quality Management System
€
490
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MDR Audit Readiness
€
620
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Medical Device Postmarket Surveillance – PMS
€
950
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