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Compare randomization and drug dispensation from IRT with EDC exposure data.
In a CDM workflow, "IXRS/IRT Reconciliation" is applied to keep data consistent and inspection-ready.
Applying "IXRS/IRT Reconciliation" inconsistently across sites or missing documentation of decisions.
How do you implement and document "IXRS/IRT Reconciliation" in a study so it is repeatable and auditable?