CEN ISO/TS 19293:2018

European foreword
Endorsement notice
Foreword
Introduction
1 Scope
2 Normative references
3 Terms, definitions and abbreviated terms
4 Dispense process and dispense event
5 Requirements
Annex A (informative) - Examples of use cases
        (from NVN-ENV 13607)
Annex B (informative) - Examples of use cases
        (other sources)
Annex C (informative) - Dispensing processes - Examples
        and variation
Annex D (informative) - Identifying dispensed products
        across jurisdictions - Using IDMP And national identifiers
Annex E (informative) - Use case-specific constraints of
        using dispense record
Annex F (informative) - Informative typical data
        structures - Elements and vocabularies
Bibliography

ISO/TS 19293:2018 specifies requirements for a record of a dispense of a medicinal product.It is intended to be adopted by detailed, implementable specifications, such as interoperability standards, system specifications, and regulatory programs.ISO/TS 19293:2018 applies to information systems in which a dispense of a medicinal product is registered, and the systems that consume such information. These systems are usually in pharmacies or other healthcare institutions. This document does not necessarily apply to non-pharmacy shops or other non-clinical systems (e.g. supermarket cashiers).The scope of ISO/TS 19293:2018 includes the activities relating to the dispensing of a medicinal product and the information content for the capture of structured information produced in those events.These activities include any actual dispense, cancellation or other outcome that may have occurred at the time of planned or actual dispense. In other words, the dispense record also contains information that medication was expected to be dispensed but was not dispensed.