National Clinical Audit Platform
48000000
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Software package and information systems
A single platform to support national clinical audit and implant registers, enabling rapid implementation of new audits, offering opportunities to improve data collection interfacing, validation and reporting. The system will also need to meet new regulatory requirements for implants. EU Directive - Medical Devices Regulation (MDR) (EU) 2017/745 and In-Vitro Diagnostics Regulation (IVDR) (EU) 2017/746 regulations.