Public Deliverables
WP 01
D1.1 Gap Analysis of Existing and Need for New Standards and Profiles
WP 01
D1.2 Requirements for a new ISO logical model
WP 01
D1.5 ISO IDMP Handbook
WP 02
D2.1 Endorsed Implementation Plan for Substance Management
WP 04
D4.1: Austria: Progress report on implementation
WP 04
D4.2 ESTONIA: Progress report on implementation
WP 04
D4.3 Finland: Progress report on refactoring or new build of national IT systems, migration of national data, and data interfaces to EMA’s SPOR
WP 04
D4.4: Germany: Progress report on implementation
WP 04
D4.5: Ireland: Progress report on Implementation
WP 04
D4.6: Norway: Progress report on implementation
WP 04
D4.7: SPAIN: Annual progress report on refactoring the national IT system, migration of national data and data interfaces to EMA´s SPOR
WP 04
D4.8: Sweden: Progress report on factoring or new build of national IT systems, migration of national data, and data interfaces to EMA’s SPOR
WP 04
D4.9: Belgium progress report on refactoring of the internal AFMPS Medicinal Product databases, alignment with SPOR, and provision of IDMP compatible data feed for national eHealth organisations
WP 04
D4.10 Croatia: Progress report on refactoring or new build of national IT systems, migration of national data, and data interfaces to EMA’s SPOR
WP 04
D4.11: Portugal: Progress report on implementation
WP 05
D5.1: Business requirements for the adoption of IDMP in eHealth Services
WP 05
D5.2: Guidelines for IDMP-based Cross-Border ePrescription / eDispensation & Patient Summary
WP 08
D8.1: Report on the link between IDMP and Pharmacotherapeutic Groups and the Need for Medical Data in Pharmacotherapeutic Audit (M22)
WP 08
D8.3: Protocol and Statistical Analysis Plan for Proof of Concept Studies
WP 08
D8.7: IDMP Coding Principles and Guidance for ICSRs
WP 10
D10.1: Assessment Framework Socio-Economic Impact
WP 10
D10.4: Review report of the GDPR and other legal requirements
WP 12
