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Feb 06, 2024 9:00 AM - Feb 06, 2024 1:00 PM

Short Course: Driving IDMP Readiness and Compliance: Impact, Business Benefits, Strategies, and Application of AI

This is a Virtual Pre-Conference Short Course in conjunction with the Regulatory Submissions, Information, and Document Management Forum


This Short Course will be offered virtually – Join from anywhere! *This Course requires an additional registration fee. You do not need to be registered for the Forum to attend*


The Short Course starts with a general update on the global identification of medicinal products (IDMP) implementation, including a deep-dive into the new European pharmaceutical legislation with an impact assessment from Industry on the practical implications. Instructors will discuss the business advantages of IDMP and why it is important for companies to transfer to IDMP in their company before it will become mandatory in authorities. Attendees will gain knowledge and learn to define how IDMP compliance requires a data management strategy that includes data cataloguing, data governance and data quality and the harmonization of data across the drug development lifecycle. Finally, all will be able to demonstrate applying AI to empower IDMP compliance using an innovative AI-based solution to tackle the challenges posed by IDMP regulations, which demand compliance amidst intricate data issues, with a case study illustrating a practical utilization of AI in ensuring IDMP compliance.


Registered attendees for this virtual Short Course will receive access to the course recording for 2 full months post-course! This allows you to remain flexible with your schedule and not worry if you need to step out momentarily. Have a conflict with the dates of the course, but are interested in the content? Register anyway and you will receive access to the recording!


Receive $150 off your forum registration by registering for any combination of at least two short courses and/or primers as well as the main forum. Purchases must be made at the same time to receive the discount. Discounts will be reflected on the last page of the cart.

Learning objectives

At the conclusion of this course, participants should be able to:
  • Define what is in scope for IDMP
  • Plan for the impact of the implementation of IDMP data standards on Regulatory Affairs on a global level
  • Evaluate and discuss the impact on internal processes and systems
  • Apply AI-driven confidence metrics to enhance manual quality checks, ensuring IDMP adherence accurately

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