Why Does the Pharmaceutical Industry Need an EDM Reference Model?
The EDM Reference Model is a document management initiative aimed at developing a taxonomy/metadata reference model that can ultimately be shared by biopharmaceutical organizations as a common starting point for building sustainable, shareable EDM repositories. This free webinar will provide details of this model and its benefits to the biopharmaceutical industry.
June 17, 2009
11:00 AM-12:00 PM EDT
10:00 AM-11:00 AM CDT
9:00 AM-10:00 AM MDT
8:00 AM-9:00 AM PDT
17:00-18:00 CET (EUROPE)
Register online – www.diahome.org - enter keyword 09230.
This free webinar is sponsored by the DIA Document and Records Management SIAC Working Group in an effort to generate feedback from attendees for improvements to and implementation of the EDM Reference Model.
Featured Topics
- Partnerships, Mergers and Product Acquisitions – Value of Document Exchange
- Benefits of a Common Content Model for Documents Efficiency and Cost Savings
- Streamlined and Cost-effective Business Processes between Pharma and its Service Providers
- Reduced Work Required to Integrate Content for Mergers and Product Acquisitions
- Affordability of EDM System Implementation
Moderator
JAMES M. AVERBACK, MS
Life Science Integration Partners
Presenters
MICHELLE HERRERA FOSTER, PhD
Principal, Senior Regulatory Affairs Consultant
CTD Quality Consulting
KENNETH R. VANLUVANEE
President and CEO
Apyx, Inc.
JOHN AIKEN, PhD
Director, Regulatory Operations
Gilead Sciences
SEAN HEALY
Publishing Technologies Team Lead
Pfizer Inc.
