Course Overview

The Identification of Medicinal Products (IDMP) initiative is transforming how medicinal product data is managed, standardised, and exchanged across global regulatory systems. The ISO IDMP standards (ISO 11615–11617, ISO 11238, ISO 11239, and ISO 11240) are designed to harmonise product information worldwide, driving data quality, traceability, and regulatory efficiency.

This intensive one-day course provides regulatory, data, and IT professionals with a clear understanding of the IDMP data model, EMA’s SPOR framework, and the evolving EU implementation roadmap. Participants will learn how to interpret IDMP standards, assess data readiness, and plan a step-by-step implementation strategy aligned with their organisation’s target operating model (TOM).

The training combines technical insight with practical examples and use cases to help attendees understand how to transition from existing xEVMPD processes to IDMP compliance. By the end of the day, participants will be equipped with the knowledge to design a structured approach to IDMP preparation, execution, and maintenance.

Learn more about how we deliver live online training.

Key Learning Objectives

• Understand the purpose, scope, and structure of the ISO IDMP data model.
• Explain the need for standardised product identification and the global context of IDMP.
• Review the current implementation status of IDMP within the EU and internationally.
• Interpret the EU Implementation Guide and EMA’s SPOR (Substance, Product, Organisation, Referentials) data framework.
• Evaluate use cases demonstrating IDMP’s impact on regulatory processes and data governance.
• Understand GIDWG use cases and implications for the Target Operating Model (TOM).
• Assess the organisational and system changes required for regulatory optimisation.
• Identify key steps to prepare for and maintain long-term IDMP compliance.

Who Should Attend?

This course is designed for professionals working in:

• Regulatory Affairs and Operations
• Data Management and Regulatory Informatics
• Regulatory Information Management (RIM)
• Quality Assurance and Compliance
• IT Systems and Regulatory Data Integration
• RIM and eSubmissions
• Project or Change Management supporting IDMP or SPOR initiatives

It is suitable for both large organisations preparing for structured data migration and SMEs seeking practical guidance for efficient IDMP implementation.

Format, Dates & Times

Find out when this course is running so you can plan your training. Scroll down to view the full agenda.

20 & 21 May 2026

1-Day Live Online Training
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3 & 4 November 2026

1-Day Live Online Training
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Course Times

For live online delivery, both sessions start at 1:00 PM (UK time) and finish at 4:00/4:30 PM (UK time).

Group Discount

If you want to train a small group, we offer a group discount between 5% and 50% depending on the course and number of attendees.

For a quote, complete our contact form by following the link. Get in touch.

Customised Team Training

We also design and deliver fully customised team training focused on your products, processes, technologies and challenges. This is ideal for specific training requirements or larger groups. Please get in touch with us for more information.

For more information, complete our contact form by following the link. Get in touch.