Updated Radioactive Drug Research Committee (RDRC) (markdown)
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Coming soon...
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### Business Requirements
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- Research teams using a new medical device in their clinical research must complete and submit the New Medical Device form to Clinical Engineering for review prior to the study being submitted for IRB-HSR approval.
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- The Coordinator will be able to upload one or more approved New Medical Device forms.
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### Protocol Builder Interface
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This workflow relies on the presence of the _New Medical Device Form_ on the PB coversheet.
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### CRC1 Stats
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This workflow does not have any CRC1 stats.
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### Study Dashboard Menu Dependencies
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| State | Condition |
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|:--------:|:---------:|
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| required | _New Medical Device Form_ document on PB Coversheet |
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| hidden | _New Medical Device Form_ document not on PB Coversheet |
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### Workflow Description
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The workflow allows the Coordinator to upload one or more approved New Medical Device forms.
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![image.png](https://images.zenhubusercontent.com/5f0623d8a1d620a9f39301dc/3a70337b-98c1-41fd-a417-a0139e60aef6)
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### Documents
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No documents are produced from this workflow.
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