L
o For positive patient identification, either the patient’s name and identification number or a unique patient identifier and identification number --> [Part of CCDA header <recordTarget>]
o The name and address of the laboratory location where the test was performed
o The test report date
o The test performed
o Specimen source, when appropriate
o The test result and, if applicable, the units of measurement or interpretation, or both
o Any information regarding the condition and disposition of specimens that do not meet the laboratory’s criteria for acceptability
o Pertinent “reference intervals” or “normal” values, as determined by the laboratory performing the tests, must be available to the authorized person who ordered the tests and, if applicable, the individual responsible for using the test results
o The information for corrected reports