EU MDR 2017/745
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What is EU MDR 2017/745?
EU MDR 2017/745 refers to the European Union Medical Device Regulation (MDR) 2017/745. It is a regulation that sets out the requirements for placing medical devices on the EU market. It covers aspects like device classification, conformity assessment, clinical evaluation, post-market surveillance, and traceability, with the aim of ensuring the safety and performance of medical devices and protecting public health.
What other technologies are related to EU MDR 2017/745?
EU MDR 2017/745 Complementary Technologies
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Which job functions commonly mention EU MDR 2017/745?
Public Policy
47 Public Policy jobs mention EU MDR 2017/745
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jobs on Sumble
Auditor
15 Auditor jobs mention EU MDR 2017/745
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jobs on Sumble
Quality Assurance
41 Quality Assurance jobs mention EU MDR 2017/745
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jobs on Sumble
Compliance
9 Compliance jobs mention EU MDR 2017/745
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jobs on Sumble
Quality Engineer
6 Quality Engineer jobs mention EU MDR 2017/745
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jobs on Sumble
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