Health informatics — Clinical particulars — Core principles for the harmonization of therapeutic indications terms and identifiers

Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging

Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of units of measurement

Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated medicinal product information — Amendment 1

Health informatics — Identification of medicinal products — Core principles for maintenance of identifiers and terms

Health informatics — Business requirements for a syntax to exchange structured dose information for medicinal products

Health informatics — Requirements for electronic prescriptions

Health informatics — Identification of medicinal products — Implementation guidelines for ISO 11239 data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging

Health informatics — Medication management concepts and definitions

Health informatics — Requirements for medication safety alerts

Health Informatics — Requirements for a knowledge base for clinical decision support systems to be used in medication-related processes

Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of Manufacturing Process & Controls Information of products and substances for pharmaceutical industry

Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 1: Framework for adverse event reporting

Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 2: Human pharmaceutical reporting requirements for ICSR