
Elementi essenziali dei regolamenti europei sui dispositivi medici (MDR UE) - 2017/745
Elementi essenziali dei regolamenti europei sui dispositivi medici (MDR UE) - 2017/745
What You Will Learn In This Free Course
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Get your PlanLearners Who Took This Course Also Enrolled In
- ISO 13485:2016 - Quality Management Systems for Medical Devices
- ISO 14971:2019 - Risk Management Application on Medical Devices
- 21 CFR Part 820 - Fundamentals of Quality System Regulation (QSR)
- Fundamentals of US FDA Medical Device Submission Process
- Fundamentals of EU IVDR Regulations for In-Vitro Medical Devices
- ISO 9001:2015 - Quality Management System (QMS)
- Good Clinical Practice - ICH Guidelines E6 R2
- Document Control: From Principles to Practice