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This document specifies the business requirements for the structured content of structured or semi-structured dose instructions for recording dose instructions in the electronic health record (EHR), supporting clinical decision support, and in exchanging medication orders, as applicable to primary, secondary and tertiary care. Comprehension of dose instructions by the patient is an overarching consideration for patient safety and the best patient outcomes. Related factors are discussed, but are not part of the primary scope. This document does not define an information model, except to the extent that those information model concepts are necessary to define business requirements. The responsible committee for this standard is NA 063-07-03 AA "Terminologie" ("Terminology") at DIN.
This document has been replaced by: DIN CEN ISO/TS 17251:2024-11 .