A Collaborative Approach to Managing Clinical Trials
Learn How A CTMS Can Improve Your Clinical Trial Processes in a Free One Day Seminar!
Winchester Business Systems continues its nationwide seminar series on the benefits of electronic clinical trial management at the IBM facilities in Lexington, MA on Tuesday, June 5, 2007. Discussed at the seminar will be areas of potential savings through a centralized, shared approach to trial management. This complimentary, full-day event is invaluable to any life science professional involved with trial management.
Despite the benefits and opportunities that electronic clinical trials can offer, many organizations are finding it difficult to predict and capitalize on the benefits that can be realized by utilizing technology to manage trials. Your organization needs full participation by all departments – planning, operations and finance – to successfully manage Phase II and III trials on a global basis.
The current systems used by most organizations – individual spreadsheets and disconnected databases, cannot support the increased volume and complexity of these trials. In fact, they can significantly slow down the time to close-out and increase the risk of FDA rejection due to incomplete or non-compliant information. Learn how a centralized, collaborative system can increase accuracy, reduce time and improve the overall clinical development process. In this seminar, you’ll get the latest perspectives on the following topics:
- How to effectively manage and retain good investigators by providing easy-to-use tools to manage trials and by accurate and timely payment.
- How to realize “Early Warning” signals of potential bottlenecks and barriers to trial progress.
- Creating an integrated and collaborative work environment for clinical trial management designed to help streamline and automate the operations of clinical trials and enable better and faster reporting.
- A review of changes to SOPs that can improve clinical operations when moving to an electronic environment.
- Areas of potential savings available through a centralized, collaborative approach to trial management.
- How to compute your potential ROI in implementing a CTMS.
Who Should Attend?
Clinical Project Managers, Vice Presidents and Directors of Clinical Operations, Financial Managers who are responsible for clinical budgets, CIO’s and IT Managers who support clinical operations for biotechnology, pharmaceutical, or medical device manufacturers or at CROs.
If you are unable to attend this seminar, look for details coming soon on additional events to be held Fall 2007 in San Mateo, CA and Princeton, NJ.
About Your Workshop Leaders:
Michael O. Regentz, CSI, CPIM, Managing Director, Winchester Business Systems, possesses experience in the pharmaceutical and medical device industries architecting closed-loop systems for clinical trials and quality systems.
Mark Levine, Vice President, Business Development & Marketing, Averion International Corp. oversees the Averion’s business development, client management and marketing teams.
