N H S Shared Business Services
RAIDIR Proposal for Regulatory Services
This is a contract result notice, not an open opportunity. Details from the official award data.
This sits below the typical range for Office & Computing Equipment contracts — a smaller, more accessible award. Based on 8,857 valued Office & Computing Equipment tenders in our corpus.
ETHOS Ltd has recently been engaged to explore providing Clinical Risk Management services relating to compliance with DCB0129: Clinical Risk Management: its Application in the Manufacture of Health IT Systems and UK MDR 2002.
RAIDR is the UK's leading health intelligence tool and is used throughout the country.
It underpins our approach to Population Health Management using advanced analytical techniques which link and aggregate data to provide comprehensive cohort analysis.
RAIDR puts you in total control, with all the information you need at your fingertips allowing sophisticated navigation, manipulation, and the exploration of multiple datasets.
There is a regulatory requirement to support the classification of RAIDR dashboards as a class one medical device.
To support the ongoing development of the RAIDR dashboards there is a requirement to build up the internal skills and knowledge to support this ongoing requirement.
Essential skills do you need from the supplier in order for you to complete the project successfully: • Knowledge of NHS clinical safety standards DCB0129 and DCB0160 • Understanding of MHRA medical device standards and regulations
What the notice asks for
And aggregate data to provide comprehensive cohort
and aggregate data to provide comprehensive cohort analysis.
There is a regulatory requirement to support
There is a regulatory requirement to support the classification of RAIDR dashboards as a class one medical device.
To support the ongoing development of
To support the ongoing development of the RAIDR dashboards there is a requirement to build up the internal.
Skills and knowledge to support this ongoing
skills and knowledge to support this ongoing requirement.
Sentences from the notice that state an obligation, surfaced automatically and shown in the order they appear. Not an exhaustive list — always confirm against the tender documents.
What this notice demands of you
1 named, none in explicit obligation language. Each one is quoted from the notice.
Understanding of MHRA medical device standards and regulations
Matched against the notice text, so this is a floor — the tender pack will demand things the notice never mentions. “Says must” means the quoted sentence itself used obligation language; anything ambiguous is left as a mention.
Make the case to bid
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- OCID
- 50673ca0-d8f1-491e-ad2e-e18fc49160a2
- Stage
- contract · Contract
- Source
- Contracts Finder
- Buyer ref
- SBS22-247
Contains public sector information licensed under the Open Government Licence v3.0. Source data © Crown copyright.
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