Regulatory Information as Part of Future Big Data Architecture

31 March 2020

To eliminate the risks associated with this type of traditional authoring, data needs to be stored in one centralized system. With a single-source system, individuals and teams throughout the organization will have access to the most up-to-date information allowing for easy creation of new documents.

In this webinar, industry thought leader and Amplexor subject matter expert, Romuald Braun, will discuss the parts of a Regulatory Information Management (RIM) system, including documents, data, and processes. He will also explain how the approved master data within the RIM system becomes reusable content building blocks; and how these building blocks can reduce the complexity and increase compliance of newly created content.

About the Presenter

Romuald Braun, Vice President, Strategy - Amplexor Life Sciences
Romuald's 25-year career to-date has been spent across roles related to Compliance, Document Management, Content Management in the Life Sciences industry – both on the client-side and in consulting, spanning delivery, sales, project, and line manager roles. His experiences bridge on-premise and cloud environments in Europe and the US.

Romuald holds a Master’s degree in Drug Regulatory Affairs from the University of Bonn (Germany) and his diploma in Data Technology from the Technical University (TU) Darmstadt (Germany).

Session A

31 March - 5:30 a.m. MDT / 12.30 GMT / 13.30 CET


Session B

31 March - 9:30 a.m. MDT / 16.30 GMT / 17.30 CET