Keep medicine identity intact across the handover.
A product description alone is a weak connection between systems. Agree the medicine and pack identifiers, catalogue source and update process before connecting purchasing, inventory or clinical applications.
- 01Identify the concept
- 02Resolve the pack
- 03Review changes
- 04Test the handover
Illustrative process—not live patient data or a clinical decision tool.
Distinguish the concept from the actual pack
Medicine concepts and physical supplier packs answer different questions. In a typical dm+d hierarchy, VTM, VMP, AMP and AMPP represent different levels of medicine identity. Map the level needed by the receiving workflow; a pack identifier is not interchangeable with every clinical concept.
- Agree the identifiers required at each interface
- Check pack sizes and units
- Review ambiguous and missing matches
Catalogue maintenance is operational work
NHSBSA maintains dm+d and publishes extracted files weekly. Your installed service still needs an agreed refresh process, change review and handling for invalid or discontinued records. A successful import is not evidence that every downstream application has applied the changes.
- Record source and imported release
- Review invalid and discontinued identifiers
- Define failed-import and rollback procedures
Interoperability needs explicit acceptance criteria
The Pharmix medicines data service can be discussed for search, mapping and application integration. Do not assume a generic FHIR or HL7 label guarantees compatibility with your specific system. Agree the message or API contract, licences, access, field mapping and error handling.
- Named system, version and interface scope
- Representative de-identified test records
- Reconciliation and exception ownership
Bring one real workflow. Leave the patient details out.
Use de-identified examples to agree product fit, configuration, responsibilities and acceptance criteria. This guide is software procurement information, not clinical or regulatory advice.
Discuss your requirementsExplore the related productNHSBSA: about dm+d. This independent reference provides background, not endorsement or certification of Pharmix. Local procedures and professional responsibilities remain with your organisation.
