| SOP | Description | Documentation |
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| Screening |
Site specific procedures outlining institutional and ICU research office procedures governing patient screening activities. |
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| Informed Consent |
Site specific instructions for seeking and conducting informed consent activities. |
|
| Enrolment |
Site specific procedures for enrolment of study patients. |
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| Follow-up |
Site specific procedures outlining the daily monitoring of study patients and follow-up of study related tests and procedures. |
|
| Adverse Event |
Site specific procedures for identifying and categorizing adverse events during the course of a clinical trial. |
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