The Consent in Front of You — Rare Disease

A Clinical Research Coordinator scenario. Setting: Site Informed Consent Process. About 9 minutes.

You are working with Participant and coordinator, A consent discussion in progress. The situation unfolds as you decide, and each choice changes what happens next.

3 scored decisions, each graded against a published rubric rather than marked right or wrong.

Competency areas assessed: D2.

Anchored to ICH E6(R3) Annex 1 §2.8.3 — ample time to consider, comprehension checked, and no undue influence.; ICH E6(R3) Annex 1 §2.8.10 — the elements to be conveyed, including the experimental nature and the allocation.; ICH E6(R3) Annex 1 §2.8.7 and §2.12.2 — the process documented in the source record, contemporaneously..

You make the decisions and are scored on them against the global GCP standard (ICH E6(R3)). Free, no account needed to try.