All Adverse Incident Reports receive confirmation of receipt and are reviewed by the Clinical Risk Management team within one (1) business day of submission, unless otherwise specified. While every report is reviewed, the level and type of follow-up may vary depending on the nature and complexity of the event.
The review process is intended to ensure that significant events receive appropriate awareness, follow-up, and coordination, while supporting consultation, collaboration, and reflective clinical practice when appropriate.
| Note: Adverse Incident Reports are reviewed during standard business hours and do not replace real-time clinical assessment, consultation, or crisis intervention. |