Why should you consider a Regulatory Platform instead of a standalone RIM solution? In less than 30 minutes, learn first steps, realistic objectives, and business benefits when implementing an end-to-end RIM.

The purpose of a Regulatory Information Management system (RIMS) is to consolidate regulatory information into one place to enable the tracking and management of registrations. This has been the same challenge for over twenty years; replacing spreadsheets and bespoke databases, and is still very pertinent today.

Regulatory Information Management is the third part of the Document Management and Regulatory Publishing triptych. These systems are intrinsically linked, sharing documents and data within a regulatory ecosystem.

Today we are seeing further momentum in the transformation of filing data and documents in unison, as structured product registrations to Health Authorities, in addition to more complex internal processes to codify and track global regulatory information.

In this presentation we will explore the benefits of a state-of-the-art end-to-end regulatory information management platform. We will see what is desirable and what is practical in 2022

• Understand the capabilities of a RIM platform

• Learn good practices for implementing processes

• Discover how to confront common challenges

• Outline initial objectives for your RIM project

• Discover proven benefits via Use Cases