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Tuesday, June 28 • 2:00pm - 3:00pm
#237: Acquisitions and Mergers: When Companies’ Regulatory Operations Systems and Processes Converge

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Limited Capacity seats available

Component Type: Session
Level: Intermediate
CE: CME 1.00; IACET 1.00; PDU 1.00 PMI 2166-000192; RN 1.00

This session will explore key aspects necessary for success when integrating regulatory operations teams as a result of mergers and acquisitions.

Learning Objectives

Discuss the necessary elements for successfully integrating regulatory operations departments during a merger or acquisition; Identify risks related to migrating information between systems; Respond to questions from others in the organization on best practices for integrating regulatory solutions.


Sarah Powell, RAC


Challenges and Business Impact Associated with Mergers and Acquisitions
Meredith K Sewell

Building a Regulatory Information Management Capability for the Next Decade: People, Process, and Technology - Case Study
Dominique E. Lagrave

avatar for Sarah Powell

Sarah Powell

President, Powell Regulatory Services
Sarah has over 29 years of experience in pharmaceutical and related regulated industries. Most recently, Sarah has worked on assisting clients with projects related to process improvements, standards development, defining filing strategies and writing and review of submission content. Prior to that, Sarah worked on projects related to implementation of regulatory solutions and has contributed to defining product strategies for industry leading... Read More →


Dominique Lagrave

Director GRAAS Operations, Global Regulatory Writing, Amgen Inc.
Dominique has over 20 years of International Regulatory Affairs experience with the last 15 years spent in Global Regulatory Operations management. | Since 2015, Dominique is a Director at Amgen where he is leading the Global Regulatory Operations organization with responsibility for RIM, Publishing and submission management. | Dominique holds a Pharm D and a Master in Regulatory Affairs from the University of Paris.

Meredith Sewell

Director, Global Regulatory Publishing, Allergan
Meredith Sewell is Allergan’s Director of Global Regulatory Affairs Operations and leads the Publishing, RIM and Archiving functions. Meredith joined the company in Irvine, CA in 2006 and in 2015, after Allergan merged with Actavis, Forest, Watson & Warner-Chilcott, she now leads a united team of 27 people in Allergan offices in the US, England, Australia, Brazil and Singapore.

Tuesday June 28, 2016 2:00pm - 3:00pm
112AB Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA