Overview

Pursuing a World Class RIM
This Solution Provider Webinar is brought to you by DIA in cooperation with Appian

Regulatory Information Management (RIM) is central to a healthy and vibrant pharmaceutical business. Pursuing world class RIM is challenging and requires careful on-going planning, coordination, and re-evaluation of new approaches plus available and emerging information technologies and related solutions. We will evaluate current and future trends, and hear from Regulatory subject matter experts and industry leaders about their approaches and what is in store for RIM.

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Featured topics

What does a World Class RIM look like
Establish today’s baseline based on extensive survey data
Where are people looking to change and invest in the next three years – where is industry headed?
How should RIM effectiveness be measured?
Case #1 - a World Class multinational pharmaceutical company designing their Regulatory Road Map
Case #2 – a World Class multinational pharmaceutical company pursuing a global view of its regulatory portfolio

Who should attend?

Professionals who work in the area of:

Regulatory Operations and Regulatory Affairs professionals
Senior Managers, Directors and above in the Regulatory Information Management space
RIM Information Technology professionals
Core consumers of Regulatory Information (affiliates, CMC, clinical, supply, manufacturing change)

Learning objectives

At the conclusion of this Webinar, participants should be able to:

Gain a comprehensive understanding of the characteristics of World Class RIM
Get familiar with the RIM environment across Life Sciences today
Know how to measure achievement of a World Class RIM
Build an understanding of the approaches of several of your peers

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Complimentary Webinar- Pursuing a World Class RIM

Overview

Featured topics

Who should attend?

Learning objectives

Be informed and stay engaged.