RAIDIR Proposal for Regulatory Services

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    "description": "ETHOS Ltd has recently been engaged to explore providing Clinical Risk Management services relating to \r\ncompliance with DCB0129: Clinical Risk Management: its Application in the Manufacture of Health IT Systems \r\nand UK MDR 2002. RAIDR is the UK\u0027s leading health intelligence tool and is used throughout the country. \r\nIt underpins our approach to Population Health Management using advanced analytical techniques which link \r\nand aggregate data to provide comprehensive cohort analysis. RAIDR puts you in total control, with all the \r\ninformation you need at your fingertips allowing sophisticated navigation, manipulation, and the exploration \r\nof multiple datasets.  \r\n\r\nThere is a regulatory requirement to support the classification of RAIDR dashboards as a class one medical device.  \r\nTo support the ongoing development of the RAIDR dashboards there is a requirement to build up the internal \r\nskills and knowledge to support this ongoing requirement.  \r\n\r\nEssential skills do you need from the supplier in order for you to complete the project successfully:\r\n\u2022\tKnowledge of NHS clinical safety standards DCB0129 and DCB0160\r\n\u2022\tUnderstanding of MHRA medical device standards and regulations",
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