  0 Table of Contents |
  1 Home |
| 2 Representing medicinal product code systems as FHIR resources |
 3 Artifacts Summary |
 3.1 Administrable product definition |
| 3.2 Ingredient |
| 3.3 Manufactured item definition |
| 3.4 Marketing Regulated Authorization |
| 3.5 Medicinal Product Definition |
| 3.6 Packaged product definition |
| 3.7 Coding |
| 3.8 Generic ReferentialTerm CodeableConcept |
| 3.9 Identifier |
| 3.10 CodeSystemName |
| 3.11 "ASP-Liste" Authorization State |
| 3.12 Medicinal Product Name Part Type |
| 3.13 The Domain Value Set |
| 3.14 The Ingredient Role Value Set |
| 3.15 The Legal Status of Supply Value Set |
| 3.16 The Marketing Status value Set |
| 3.17 The Packaging Value Set |
| 3.18 The Pharmaceutical Dose Form Value Set |
| 3.19 The Quantity Operator Value Set |
| 3.20 The Regulatory Entitlement Status Value Set |
| 3.21 The Regulatory Entitlement Type Value Set |
| 3.22 The Target Species Value Set |
| 3.23 The Units of Measurement Value Set |
| 3.24 The Units of Presentation Value Set |
| 3.25 "ASP-Liste" Authorization State |
| 3.26 Additional Medicinal Product Name Part Type |
| 3.27 Domain |
| 3.28 Domain |
| 3.29 Ingredient Role |
| 3.30 Legal Status From the Supply |
| 3.31 Marketing Status |
| 3.32 Medicinal Product Name Part Type |
| 3.33 Pharmaceutical Dose Form |
| 3.34 Quantity Operator |
| 3.35 Regulatory Entitlement |
| 3.36 Regulatory Entitlement Status |
| 3.37 Routes and Methods Of Administration |
| 3.38 Units Of Measurement |
| 3.39 Units Of Presentation |
 3.40 Authorization State Mapping |