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Bethesda North Marriott Hotel and Conference Center

Feb 08, 2016 12:00 PM - Feb 10, 2016 5:15 PM

5701 Marinelli Road, , North Bethesda, MD 20852 , USA

Regulatory Submissions, Information, and Document Management Forum

Discuss the end-to-end process for document management, publishing, and technical regulatory requirements in regulatory information management.

Session 7 Track 4 - Trends and Opportunities in Master Data Management

Session Chair(s)

Venkatraman  Balasubramanian, PhD, MBA

Venkatraman Balasubramanian, PhD, MBA

SVP and Global Head, Industry Solutions - Healthcare and Life Sciences

Orion Innovation, United States

Pharmaceutical companies have seen the increasing adoption of master data management around key corporate information such as product, customer, employee, etc. This session will start off with an overview of master data management (what and why), how master data is already used in industries such as retail, consumer goods etc., and highlight the importance of product master data in life sciences. It will be followed by a vendor perspective around master data management, especially in the light of ISO/EMA requirements around IDMP. We will also hear a sponsor’s perspective and case study on how master data management has been implemented within their organization to address various business needs, highlighting some of their successes and challenges.


Venkatraman  Balasubramanian, PhD, MBA

Master Data Management: Why Now?

Venkatraman Balasubramanian, PhD, MBA

Orion Innovation, United States

SVP and Global Head, Industry Solutions - Healthcare and Life Sciences

Laurie  Strehl

Product Master: Drug Sponsor Case Study

Laurie Strehl

Bristol-Myers Squibb, United States

Director Business Processes

Joseph  McLaughlin, MBA

MDM Strategy for IDMP, RIM, and the Broader Business Value

Joseph McLaughlin, MBA

Genpact Pharmalink, United States

Vice President

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