Online Clinical Evaluation under EU-MDR Training
Introducing industry-leading On-Demand (24/7) Clinical Evaluation under the European Medical Device Regulation (EU-MDR 2017/745) Training for Quality & Regulatory Affairs Professionals!
The European Medical Device Regulation (MDR) is a set of regulations that must be met if producing or distributing medical devices within the EU, and if you want to sell your Medical Devices in the EU.
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- ISO 9001
- ISO 13485
- EU MDR
- EU IVDR
- ISO 14971
- FDA QSR 21 CFR 820
- ISO 17025
- ISO 14001
- ISO 45001
- ISO 27001
- FSSC 22000
- Clinical Evaluation
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This online course will offer an interactive overview of Clinical Evaluation for Medical Devices & MEDDEV 2.7/1.
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