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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Online & Self-Paced Clinical Evaluation for Medical Devices Course
★★★★★ ( Reviews, Click to view)Language: English
This online course will offer an interactive overview of Clinical Evaluation for Medical Devices & MEDDEV 2.7/1.
Duration :8hrs
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