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Bethesda North Marriott Hotel and Conference Center

Feb 25, 2014 8:25 AM - Feb 26, 2014 4:00 PM

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

Regulatory Information Management 2014

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Session 5B: Tools and Technology Track - Preparing for IDMP

Session Chair(s)

Andrew Marr, PhD

Andrew Marr, PhD

Managing Director

Marr Consultancy Ltd, United Kingdom

The Identification of Medicinal Products (IDMP) standards in support of ICH M5 were published by the ISO in November 2012. The IDMP compliance challenge would be a game changer for the industry. It will not only change the compliance landscape but also result in a significant overall strategic growth for companies that truly adhere to these standards and organize their internal RIM processes around them. This session will include the FDA perspective.

Speaker(s)

Vada Perkins, DrSc, MSc

IDMP Implementation Activities: Status Update

Vada Perkins, DrSc, MSc

Boehringer Ingelheim, United States

Vice President, Global Head of Regulatory Intelligence & Policy

Wim Cypers, MPharm

Getting Ready for IDMP

Wim Cypers, MPharm

ArisGlobal, United States

SVP Regulatory

Launching a Corporate Program to Ensure Readiness for the Identification of Medicinal Products (IDMP) Standards

William Mandarino, MSc

UCB, Inc., United States

Associate Director, Product License Knowledge Management

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