Pharmaceutical Information Management 2008
www.PIMAevent.com

Are you achieving 100% patient safety and efficacy with your drugs?

Are you unable to integrate clinical testing data with the data from internal systems for different compounds?

Are you getting top line results from your electronic data management solutions?

PIMA will be a three day event focused on clinical trials data capture and integration for operational efficiency, patient safety and regulatory compliance.

DON'T MISS interacting with your colleagues in the industry who are making progress in the field of EDC and integration solutions. Hear how companies are passing products through clinical trials and regulatory approval faster while enduring fewer costs.

Pharmaceutical Information Management for electronic clinical data is a critical branch of the pharmaceutical industry. It can be a complex and multi-faceted process because it involves several networks and channels including clinical data capture, integration and management technologies. The complexity is compounded by the various types of pharmaceutical regulations and partnerships involving data integration throughout multiple departments, as well as companies.

PIMA will not only explore the methods and technologies being used today, but will also look towards the future by analyzing trends and developments within the industry. You will have the opportunity to network with industry experts as well as brainstorm where the gaps are and what new ideas have emerged.

Pharmaceutical Information Management themes and topics include:

• Creating and developing electronic clinical data capture technologies to maximize the efforts of your company
• Integrating clinical data to be used throughout various departments to streamline company procedures
• Research & Development data management
• Clinical Trials Data Management
• Reducing time and money throughout clinical trials while increasing product quality and successfully passing through regulatory approval
• Analyzing Paper vs. EDM trial comparisons

However large or small your company is, the data created throughout the lifecycle of a molecule is the most valuable piece to saving the lives of patients depending on your products.  Ensure you are maximizing your data management solutions to streamline your efforts and achieve 100% patient safety.   

Come and learn from industry experts already tackling these critical issues:

• Greg Ambra, MS, Director, CDM and Clinical Systems, Baxter Healthcare
• Gaston Farr, Senior Director, Clinical Development, Biostatics and Data Management, Targacept, Inc.
• Chris Connor, Senior Research Analyst, Clinical Development, Health Industry Insights
• Landen Bain, Liaison to Healthcare, CDISC
• Robert Musterer, Director Clinical Systems, Bayer
• Tim Joy, Associate Director, Global Clinical Data, Pfizer
• Fred Wood, Principal Consultant, Clinical Data Strategies, Octagon Research Solutions, Inc.
• Elisa Johnson, Clinical Data Manager, Novartis Pharmaceuticals
• Barry Cohen, Director, Clinical Data Strategies, Octagon Research Solutions, Inc.
• Dominique Endicott, Director of Data Operations, Research Point
• Mark Uehling, Founder & Editor, ClinPage
• Wayne Kubick, Founding Director, CDISC, Senior Vice President and Chief Quality Officer, Lincoln Technologies Group