Research / IRB
Research ethics and protocol governance — IRB reviews, participant consent, amendments and adverse-event reporting — with a printable protocol summary.
Where to find it
Research / IRB in the app drawer (model hms.res.protocol).
Key records
| Record | What it captures |
|---|---|
| Protocol | The study protocol and its lifecycle |
| IRB review | Ethics committee decisions |
| Consent / amendment / AE | Participant consent, changes and safety events |
Printing & access
Clinical documents print on the facility letterhead from each record’s Print menu. The app is shown only to staff assigned its department role (see Departments & access).
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