Patient identity is made unambiguous and traceable. At least three identifiers are approved for the record and the primary specimen label, with national health identifiers added when available; patient, specimen and service are matched; where able, the patient checks the label; the approved identifiers appear on the primary specimen and the report; secondary samples are linked back to the primary specimen; there are rules for patients who stay anonymous and for merging one patient's records held under different identifiers; identity is re-confirmed with the approved identifiers at collection, on electronic transmission of requests, and during testing, interpretation and reporting; mismatches are corrected at once; and every identification discrepancy and its correction is written into the patient's record and the incident system.
This control maps to 1 controls across 1 other frameworks. If you already hold one of them, the evidence you collected for it is the starting point here rather than new work.
Every mapping shown was judged rather than inferred from wording similarity, and the ones that failed review are published too. See the coverage reports and what was rejected.
The graph holds this control, the 1 it maps to, and the evidence behind each claim, over MCP and REST.