April 25 and 26, 2011 Join Court Square Group for a highly informative day designed to assist leaders in biotech and pharmaceutical companies in understanding good business practices associated with earning and maintaining FDA records compliance.

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 not only look at the steps that have been successful for designing, configuring, and implementing validated solutions within the confines of a regulated environment.

The day is kicked off by an internationally recognized speaker presenting an interactive Leadership Styles workshop. Following lunch, three afternoon sessions discuss good systems practices GSP® supporting FDA compliance in several critical life science operational areas, including “SharePoint in an FDA Regulated Environment”.

Life Science Leadership Day is being held at the Microsoft NERD Center, 1 Memorial Drive, Cambridge MA, 02142 on Monday, April 25, 2011, and at the Malvern PA Microsoft facility: Great Valley Corporate Center, 45 Liberty Blvd, Suite 210, Malvern, PA 19355 on Tuesday April 26, 2011. Both events are free.

Click Here for more details about the Agenda and Speakers!

To register for these events, click on one of the following:

https://www.clicktoattend.com/invitation.aspx?code=154885 for the Cambridge MA event

https://www.clicktoattend.com/invitation.aspx?code=154929 For the Malvern PA event

For more information, call or write Craig Wilson at 413-746-0054 or wilson@courtsquaregroup.com

June 22, 2011

Keith Parent, CEO of Court Square Group, will join a panel discussion during the Drug Industry Association’s (DIA) annual convention, being held in Chicago in June 2011.  Mr. Parent, a noted industry expert in the technology issues in operating in FDA regulated environments, will participate in a panel that will discuss the ethical issues and regulations involving Electronic Health Records (EHR)/Electronic Clinical Trials (ECT) information.  The panel will address questions of informed consent, EHR/ECT integration, appropriate privacy and security requirements and controls.  The session will be conducted in an interactive format, with audience participation encouraged from the start to the finish.  This will be held June 22, 10:00-11:30 AM within the IT Methods and Technologies Track 07