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DIA Workshop Features Industry and FDA for Discussion of Best Practices for Electronic Establishment Registration and Product Listing
Date:7/9/2009

ul>The SPL Vendor Showcase will provides an opportunity for attendees to evaluate a number of currently available services and tools as they are used to produce an equivalent final product. During this session, participating vendors will demonstrate their services and/or tools and present their results.

The SPL Live Q&A will allow attendees to ask key FDA representatives about electronic establishment registration and product listing regulatory content, SPL technical content, or the ESG submission process

"This one-of-kind event is the only opportunity to hear industry and FDA representatives discuss best practices for electronic establishment registration and product listing," says Program Co-chair Therese Brunone, MS, Assistant Director, Global Regulatory Operations, GlaxoSmithKline.

About the Drug Information Association (DIA)
DIA serves more than 30,000 professionals involved in the biopharmaceutical industry and regulatory affairs worldwide. Through its domestic and international meetings, training courses, workshops and webinars, DIA provides a neutral global forum for the exchange of information critical to the advancement of the drug discovery and lifecycle management processes. Headquartered in Horsham, PA, USA, and with offices in Basel, Switzerland, Tokyo, Japan, Mumbai, India, and Beijing, China, the Association is led by its volunteer-based Board of Directors and executive management team. For more information, visit www.diahome.org or call 215-442-6100.

Contact: Joe Krasowski   
215-293-5812

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Read the full story at http://www.prweb.com/releases/2009/07/prweb2621874.htm.


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DIA Workshop Features Industry and FDA for Discussion of Best Practices for Electronic Establishment Registration and Product Listing
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