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MHRA Device Safety Information – MDSI2107
MDSI2107 - Recall of BD Venflon Pro safety and Venflon Pro IV cannula
Endoscope Decontamination Document System (EDDS) (PRO-179 series)
Documentation system covering decontamination policy document and procedures covering the management of flexible endoscope decontamination lifecycle
MHRA Device Safety Information – MDSI (SC) 2105
MDSI (SC) 2105 - Recall of BD Venflon Pro safety IV cannula
Access the Statutory Compliance Audit and Risk Tool (SCART)
Access SCART to report on your health board's legal compliance.
Access the Healthcare Associated Infection System for Controlling Risk in the Built Environment (HAI-SCRIBE)
Access our HAI-SCRIBE tool to manage infection control risks in your health board.
Access climate change and sustainability tools
Access our energy and sustainability resources for health boards.
MHRA Medical Device Safety Information – MDSI2406U
Philips Respironics BiPAP A series ventilators: alarm malfunction and risk of therapy interruptions in ventilators not intended for life-support
National IT system: Scottish Cervical Call Recall System (SCCRS)
SCCRS is the central IT system that supports the Cervical Screening Programme. Staff can use this area to access relevant documentation.
Brevity and clarity
Support with online reports
Details of where you can get support for your reports.