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ABX-CRO’s quality management is certified according to ISO 9001:2015 as well as ISO 13485:2016. QDOSE® conforms to the European Medical Device Regulation (Regulation EU 2017/745) and is CE-marked as
Medical Device (Class IIa) for clinical use inside the European Union.
Outside the EU, QDOSE® can be used for research purposes only.
Medical Device (Class IIa) for clinical use inside the European Union.
Outside the EU, QDOSE® can be used for research purposes only.
