Foreword
Introduction
1 Scope
2 Normative references
3 Message exchange format
4 Conformance terminology and context
as it relates to the ISO IDMP standards and
corresponding IDMP technical specifications
5 Terms, definitions and abbreviations
6 Requirements
7 Description of the information modelling
principles and practices
8 Identifying characteristics for authorised
Medicinal Products
9 Information for an authorised Medicinal
Product
10 Identifying characteristics for Investigational
Medicinal Products
11 Information for an Investigational
Medicinal Product
Annex A (informative) - Full model - Authorised Medicinal
Products detailed diagram
Annex B (informative) - Full model - Investigational Medicinal
Products detailed diagram
Bibliography