Training: Implementing IDMP
using FHIR
Principles and concepts of ISO Identification of Medicinal Products (IDMP) and HL7 Fast Healthcare Interoperability Resources (FHIR)
Next training
Open date
Education program for stakeholders currently working on IDMP related data management/governance projects
The European Medicines Agency (EMA) has chosen the HL7 FHIR standard for the implementation of ISO IDMP. This online training course offers a solid overview of the IDMP standard, and overview of the FHIR exchange standard, as well as interactive sessions focused on the implementation of IDMP using FHIR.
The attendees are expected to follow two education blocks:
1. Principles and concepts of ISO IDMP | 2 days (5 hours p/d) | Open date
2. Principles of FHIR and FHIR in IDMP | 2 days (5 hours p/d) | Open date
It is possible to follow the 2-day ISO IDMP training only.
Learning goals
Upon completion of this training course, you will understand:
• The IDMP data model.
• The use cases in which the IDMP data model can be applied.
•
All of the EMA SPOR data services and how these relate to the IDMP data model.
• The process around EMA SPOR services based on the Target Operating Model (TOM) and the associated timing.
And will be able to:
• Plan and prepare an effective strategy for IDMP implementation to meet its deadlines.
• Describe the characteristics and contents of the core IDMP models including message exchange.
• Explain the key principles underlying the FHIR exchange standard.
• Build upon hands-on experience with FHIR gained during the training course.
• Help their organization to determine if, when, where and how they might implement IDMP using FHIR.
• Explain the developments with FHIR and the implications it has.
• Define your implementation roadmap and tools, to start defining and publishing your specifications.
Who should attend
This program is aimed at stakeholders involved with the design, development, implementation, deployment and support of ISO IDMP by using the HL7 FHIR standard. Such stakeholders are professionals currently working on IDMP implementation projects in Europe, such as: EU, SPOR, EU-SRS, SPOR, and UNICOM.
The scope of this educational offering supports IDMP Program Managers, IDMP Business/IT Project Managers, Business Analysts, Technical Data Architects, data managers, and IT Developer.
What other trainees said
83%
I would recommend this training to my colleagues
76%
The training was useful and directly applicable in my job
94%
The trainers were real experts
Our main goal is
For you to understand ISO IDMP and HL7 FHIR in IDMP
We selected two expert trainers covering all aspects of IDMP and FHIR in IDMP. This unique combination ensures you to get a practical training for a successful implementation of ISO IDMP (SPOR).
We follow up on all attendees, because we want you to understand IDMP and FHIR in IDMP. In case you feel a gap in your knowledge, we offer extra sessions and will address this gap and new developments to you.
The trainers
Lise Stevens
ISO IDMP Specialist
Lise Stevens is a regulatory and health information technology expert specializing in data standards development, training and implementation of ISO IDMP and ICH E2B(R3). She has over 30 years of experience in IT project management, data and systems analysis design, testing and implementation. She is a co-editor for ISO IDMP Technical Report on IDMP terminology maintenance principles and co-led the development of the ISO/HL7 27953 ICSR specification adopted by ICH, VICH and FDA eMDR. She successfully implemented FDA’s first iteration of ICH E2B(R3) for vaccine AE reporting and currently serves as a US expert to ANSI/ISO TC 215 for pharmacy and traditional medicines topics.
José Costa Teixeira
HL7 FHIR specialist
José Costa Teixeira is a data management and interoperability expert. José has 20 years of experience in managing and integrating IT solutions for healthcare. He has been an active contributor to several standards organizations (HL7, IHE, ISO, DICOM), also as a lead editor of normative and informative material. He has been a committed contributor to FHIR for several years. José has also helped several enterprises setup their data governance programs, where master data and data quality are an important topic. In all these areas, standards-based interoperability is a key factor and José is a strong promoter of standards to achieve business value and operational efficiency. José is currently assisting with the national implementation of FHIR in different institutions in Belgium (government and industry), from aligning the roadmaps to publishing several specifications, and setting up projects, servers and testing with the developers.
The training outline
IDMP principles and concepts
- Introduction and drivers for ISO IDMP.
- Relationships with other relevant standards: ICSR, SPL, FHIR (EMA SPOR).
- IDMP Data Models including related class models & attributes, e.g. Clinical Particulars, Organizations, Packaging, etc.
- Relevant IDMP Use Cases, both regulator as industry
EU ISO IDMP Implementation
EMA SPOR Implementation Guide
Target Operating Model (TOM) and the impact to business processes
FHIR principles and concepts
- Introduction of HL7 FHIR standard
- Emergence, resources, exchange methods and terminologies
- FHIR domain resources and logical models
- Use cases for FHIR and IDMP
FHIR implementation
- FHIR ecosystem including the FHIR maturity model
- Development of FHIR specifications
- Implementation roadmap
And more
- Interactive sessions and exercises
- Plenty of room for questions
Get ready for IDMP Implementation
Registration fee for this 4-day course is
€ 1,750 for general attendance
€ 900 for the 2-day IDMP training