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Evnia provides the Medical Device, Pharma and Biotech industries with specialised consulting services in the areas of Regulatory Affairs/Compliance, R&D and Management by transforming data and regulations into measurable actions and tailored solution
27-27 September 2022
The EU MDR 2017/745 was published in May 2017 with a transition period of three years which was extended by one additional year to address COVID 19 restrictions and limitations. This additional year was taken away from the predefined grace period in
Event Ended
Spain
Paid
Barcelona