Pharmaceutical and biotech companies have been facing increasing demands to improve their organizational effectiveness through information sharing and collaboration. At the same time, there is an important need for a controlled document management system that is compliant with FDA regulations. In this conference, our speakers look at the steps necessary to design and implement Microsoft SharePoint within the confines of a regulated environment. The presentation discusses various solutions, with a special focus on regulatory needs at various stages of the drug development lifecyle.
Speakers John Postle and Cary Cyr explain how to achieve ongoing compliance through the use of SharePoint as a validated application in a qualified environment. They also present a real-life case study from Tufts Medical Center, which illustrates how research laboratories are using SharePoint for collaboration.
Using SharePoint in an FDA-Regulated Environment is being presented by John Postle & Cary Cyr, Vice President, Life Science Enterprise & Senior SharePoint Specialist, with Court Square Group and airs on Thursday, October 22, 2009. For more details or to register, please visit our site at www.fxconferences.com
