Updated Radioactive Drug Research Committee (RDRC) (markdown)

calexh-sar 2021-04-02 20:33:27 -04:00
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Coming soon...
### Business Requirements
- 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.
- The Coordinator will be able to upload one or more approved New Medical Device forms.
### Protocol Builder Interface
This workflow relies on the presence of the _New Medical Device Form_ on the PB coversheet.
### CRC1 Stats
This workflow does not have any CRC1 stats.
### Study Dashboard Menu Dependencies
| State | Condition |
|:--------:|:---------:|
| required | _New Medical Device Form_ document on PB Coversheet |
| hidden | _New Medical Device Form_ document not on PB Coversheet |
### Workflow Description
The workflow allows the Coordinator to upload one or more approved New Medical Device forms.
![image.png](https://images.zenhubusercontent.com/5f0623d8a1d620a9f39301dc/3a70337b-98c1-41fd-a417-a0139e60aef6)
### Documents
No documents are produced from this workflow.