Technical Documentation within the MDR conformity assessment procedure
Technical Documentation within the MDR conformity assessment procedure
Different timeline services are supplied to serve our customers according to their individual readiness. Parts of the MDR technical documentation assessment can be expedited to a service, that is processed with the highest priority. The diagram below shows a comparison of our basic service model for certification with our Expedited Service options.
Please note that fast track services options are subject to availabilities of appropriate resources.

The given timelines are target timelines of the planning model. Individual timelines may differ. Fast track services available in selected regions.
According to the Medical Device Regulation (EU) 2017/745 (MDR)
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Opportunities and challenges in applying the EU AI Act 2024/1689 to AI-driven medical technologies
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