Deployment of the preliminary platform on the cloud
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The cloud layer will be deployed in its current form as an application through IaaS hosting model.
Business, System & Software Requirements Specification Documents
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The BRS section of the document will be prepared as a structured outline of the executive summary, objectives, stakeholders, broad requirements from end-user's point of view, constraints and what’s expected throughout the planned lifecycle.The SysRS section of the document will be prepared to describe the features and behavior of the planned system while indicating minimum hardware - software specifications, analyzing functional and non-functional requirements. The SwRS document will be prepared to detail the specific requirements of the connectivity platform to be developed. These requirements will be derived from the ones in SysRS and will specify the functional, external interface and non-functional software requirements (regarding performance, security, usability, scalability)
Project handbook
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Incidental/unexpected findings policy
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High and Low-Level Software Design Document
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The HL SDD will be prepared to trace the requirements to HL design entities and identify the parent/child structural relationships for the platform. The LL SDD will be prepared to directly reference to the SwRS with parameters, assumptions, dependencies, constraints and guidelines for building the platform. It also includes the development methodology adopted, architectural decisions and patterns chosen, system definitions, subsystems, modules, interfaces, external interfaces,processes, and descriptions of the data design.
D2 and D3 end-user feedback report
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UMC will test the EEG patch (D2) and fNIRS patch (D3) prototypes in healthy volunteers and suspected stroke patients with the involvement of ambulance paramedics. Feedback will be reported to EUT/TrianecT (D2) and UOULU (D3) as input for the next prototype.
Clinical studies: Initiation package
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This activity will be aimed to monitor the ethical issues of the entire project. In addition to medical ethics, compliance with EU ethical guidelines for reliable AI should be ensured. The POC4TRIAGE consortium will adopt the EC’s ethical guidelines in consultation with the ethics committees and will provide feedback to the relevant WPs. A framework for data security and privacy will be built through interactions with hospital security specialists and ethics committees.
