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Page info

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title
title

Pre Interview:

Item

Information/Response

Date

12/09/2009

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Requirement # unique id <SemCon Ops Initiative>.<analysts

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initials><requirement

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number>

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e.g.

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Init1dbw1

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(eventually linked to Use Cases)

Init1dbw3

Originator/Customer's

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Name

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:

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CBIIT

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-

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Margaret

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Haber                                                                                        

Originator/Customer's

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Company

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:

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HL7

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draft

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CIC

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MDR requirements

Stakeholder Community:
Enter appropriate category of stakeholder from Primary Stakeholders:  

  • Software and Application designers and architects
  • Software and Application engineers and developers
  • Scientific and medical researchers
  • Medical research protocol designers
  • Clinical and scientific research data and metadata managers
  • Clinicians
  • Patients
  • Medical research study participants
  • Broader Stakeholders: caBIG® Community WS NIH projects and related commercial COTS vendors (caEHR, SDO's (HL7, CDISC); International Collaborators (e.g NCRI, cancerGrid, China), Government and regulatory bodies (FDA, CDC, ONC)
    (link to view SemConOps Stakeholders description).

SDO

Summary of requirement pre-interview, by Reviewer:

Support for interoperability between groups with MDRs; Collaboration tools for reviewing similar standards and making refinements to final standard; User friendly Browser; Easy way to create data elements from line of business artifacts such as a spreadsheet or database description; Need to have private and public content in the MDR;

Requirements include functional and non-functional (would like to be involved in the requirements process, UI design/feedback sessions for browsers, etc.)

Recommended Next Step Enter one: Follow-up interview, Observe, Use Case Template (text), Use Case Model (formalized/UML diagram), Group Discussion, Prototype, Waiting Room

Review document, schedule interview/questionnaire when Init 1 resources are on board (full time project Business Analysts)


Wiki Markup
 requirements \\ |
| *Stakeholder Community*: \\
Enter appropriate category of stakeholder from Primary Stakeholders:&nbsp;&nbsp;
* Software and Application designers and architects
* Software and Application engineers and developers
* Scientific and medical researchers
* Medical research protocol designers
* Clinical and scientific research data and metadata managers
* Clinicians
* Patients
* Medical research study participants
* Broader Stakeholders: caBIG® Community WS NIH projects and related commercial COTS vendors (caEHR, SDO's (HL7, CDISC); International Collaborators (e.g NCRI, cancerGrid, China), Government and regulatory bodies (FDA, CDC, ONC) \\
_[_(link to view SemConOps Stakeholders description_|Semantic Infrastructure Concept of Operations Stakeholders])._ | SDO \\
\\ |
| *Summary of requirement pre-interview, by Reviewer:* | Support for interoperability between groups with MDRs; Collaboration tools for reviewing similar standards and making refinements to final standard; User friendly Browser; Easy way to create data elements from line of business artifacts such as a spreadsheet or database description; Need to have private and public content in the MDR; \\  \\
Requirements include functional and non-functional (would like to be involved in the requirements process, UI design/feedback sessions for browsers, etc.) \\ |
| *Recommended Next Step* Enter one: Follow-up interview, Observe, Use Case Template (text), Use Case Model (formalized/UML diagram), Group Discussion, Prototype, Waiting Room | Review document, schedule interview/questionnaire when Init 1 resources are on board (full time project Business Analysts) \\ |
\\
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