Reprocess of Single Use Devices: EU MDR Requirements
Article 17 of the EU MDR 2017/745 provides comprehensive guidelines regarding the requirements for the reprocessing of single-use devices. The…
ISO 17511: Metrological Traceability for IVD Medical Devices
Recently, a new version of ISO 17511 has been published, bringing forth updated requirements for ensuring metrological traceability in In-vitro…
