Learning · Course · C-RUN-02
Audit Replay
This course teaches participants how to reconstruct a sequence of events from logs and supporting materials so that a decision can be explained after the fact without guesswork or omissions. It is relevant whenever teams must not only notice a problem, but show what happened, in what order, and with what residual risk.
| Fact | Value |
|---|---|
| Catalog queue | First queue (P1) (course catalog queue) |
| Difficulty | Foundational |
| Audience | Clinical, engineering, research, and operational teams that need traceability |
| Duration | 5 hours |
| Format | 2 learning modules, 1 practical exercise, final quiz |
| Result | Course Badge and a practical-work materials packet |
What the Course Covers
| Block | Content |
|---|---|
| Module 1 | Event timelines, the quality of supporting materials, and the rules of disciplined review |
| Module 2 | Incident closure, residual risk, and the requirements of audit traceability |
| Practical exercise | The participant assembles an incident note that is sufficient for both internal and external review |
| Final quiz | 10 questions, 85% passing score |
After the Course You Will Be Able To
- reconstruct the logic of a decision from the available logs and materials;
- assess whether the evidence is sufficient for a confident review;
- record residual risk after incident closure;
- prepare a careful explanation of an event for different roles.
How the Course Runs
This course uses the IHA (Instant Health Assessment — a series of papers on instant health assessment that the platform’s terminology partly derives from) runtime terminology: Runtime library, Compute core, stateless and stateful analyzer contours, and readiness evidence.
Course Boundaries and What Comes Next
The course confirms the ability to reconstruct a sequence of events and document an incident review. It does not grant the right to approve a release, authorize delivery, or make a clinical decision unilaterally. A Course Badge is not a Program Certificate and not delivery eligibility: both remain separate steps — see “What Happens After a Program” on the training hub.
- OEM Integration Program (P-OEM)
- Clinical Operations Program (P-CLN)
- Knowledge Authoring Program (P-KA)
- Knowledge Approval Program (P-KAP)
- Release Operations Program (P-RO)
- Research Program (P-RES)
- Medical Science Program (P-SCI)
Discuss whether this course fits your team. Contact us