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Session 6, Track 1: DIA RIM Reference Model V2.0 catches FHIR!
Session Chair(s)
Jennifer Dames
Director, RA Submission Management
Abbvie, United States
In this session, we will provide an overview of the updates to the RIM Reference Model in 2024. We will discuss physical implementation specifications for data requirements for organizations considering a RIM initiative and explain how to create a physical model to support migration activities between RIM systems and also real time integrations between RIM and other regulatory systems.
Learning Objective : At the conclusion of this session, participants should be able to:- Gain understanding of updates to DIA RIM Reference Model (V2.0)
- Understand use of the model as data requirements specification for an organization considering a RIM initiative and/or a regulatory data hub
- Explore how the model could be utilized as a data migration map between different RIM systems and/or in an M&A scenario
Speaker(s)
Overview and Highlights of RIM Reference Model V2.0
Venkatraman Balasubramanian, PhD, MBA
VB Insights, LLC, United States
Healthcare and Life Sciences Strategic Advisor
RIM Reference Model V2.0: Deep Dive
John Jones, MBA
EntiTech Solutions, United States
Chief Executive Officer
Leveraging the RIM Reference Model in a Small Company Setting
Vahe Ghahraman, PhD
Apellis Pharmaceuticals, Inc. , United States
Senior Director, Global Regulatory Operations Head