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PD CEN ISO/TS 19256:2017 Health informatics. Requirements for medicinal product dictionary systems for health care, 2017
- 64_e_stf.pdf [Go to Page]
- European foreword
- Endorsement notice
- 30333881-VOR.pdf [Go to Page]
- Foreword
- Introduction
- 1 Scope
- 2 Normative references
- 3 Terms and definitions
- 4 Abbreviated terms
- 5 Boundary between MPD-systems and IDMP, ancillary information to build an MPD-system and local implementation
- 5.1 Boundary between MPD-systems and IDMP
- 5.2 Boundary between MPD-systems and ancillary information to build an MPD-system
- 5.3 Boundary between MPD-systems and local implementation
- 5.4 Content of the MPD-systems in terms of product coverage
- 5.5 Definition of Medicinal Product Dictionary MPD-systems
- 5.6 Benefits of the Technical Specification
- 5.7 Target users for the Technical Specification
- 6 Positioning of Medicinal Product Dictionary Systems for Healthcare
- 6.1 Base materials for MPD-systems
- 6.1.1 Relation with ISO IDMP standards
- 6.1.2 Relation with health/clinical/pharmacy information systems, decision support, EHR and dose instructions
- 6.1.3 Relation with EHR-S FM
- 6.2 Use cases for requirements for an MPD-system
- 6.2.1 Prescribing use case
- 6.2.2 Dispensing use case
- 6.2.3 Administration use case
- 6.2.4 Recording medication history use case
- 6.2.5 Reconciling medication list use case
- 6.2.6 Ordering and supply chain (logistics) use case
- 6.2.7 Analysis, statistics, and pharmacoepidemiology use case
- 6.2.8 Electronic data exchange of medicinal product information between healthcare systems and/or related systems, i.e. reporting use case
- 6.2.9 Reimbursement use case
- 6.2.10 Clinical research use case
- 6.2.11 Tracking and tracing for patient and public safety use case
- 6.2.12 Pharmacovigilance use case
- 6.2.13 Patient safety through linking personal data with the decision support system on medicinal products use case
- 6.2.14 Migration use case
- 7 The Functional Requirements for MPD-systems
- 7.1 Introduction
- 7.2 Goal of an MPD system
- 7.3 Normative content
- 7.3.1 Content of regulated medicinal products
- 7.3.2 Prescription
- 7.3.3 Dispensing
- 7.3.4 Administration
- 7.3.5 Recording and reconciliation
- 7.3.6 Order and supply chain and logistics
- 7.3.7 Analysis, statistics, pharmacoepidemiology, and clinical research
- 7.3.8 Ensuring patient safety through linking personal data with the decision support system on medicinal products
- 7.3.9 Interaction with reimbursement systems
- 7.3.10 Interaction of MPD-systems with pharmacovigilance systems
- 7.3.11 Data exchange and technical functions
- 7.4 Governance
- 7.5 Maintenance
- 7.5.1 Regular maintenance processes of the MPD-system
- 7.5.2 Interaction with regulatory information
- 7.6 Localization
- Annex A (informative) IDMP series in context, serving this Technical Specification
- Bibliography [Go to Page]
