SharePoint for Pharma Webinar Series
SharePoint is being used more and more in the Life Sciences arena as a collaborative platform which allows us to manage documents and records, business processes, user interactions and business intelligence. Given its user friendliness and multitude of potential applications, both regulated and non-regulated, the use of SharePoint can grow rapidly across the enterprise. It is imperative to properly plan and manage your SharePoint environment so as to be able to leverage all of the benefits of such a platform whilst maintaining control and scalability in regulated environments.
Montrium will be presenting a series of free informative webinars on the validation and use of SharePoint within regulated pharmaceutical environments. The webinar series will focus on compliance and management of SharePoint whilst giving real-life examples of how SharePoint can be deployed and managed within life sciences companies. The first webinar will be presented by Paul Fenton, VP Pharmaceutical Processes and Technology on April 23rd. The webinar series will include the following subjects:
June 18th 2010 – 11am-12pm EST – Going Paperless – Executing Validation of GxP Systems Electronically using SharePoint
Presented by Gianna De Rubertis, GxP Systems Validation Coordinator, Montrium Inc.
With the emergence of enterprise technologies and content management systems such as SharePoint, the documentation burden associated with paper-based validation can be greatly alleviated and even eliminated. In this session, you will take a glimpse at the future of validation of GxP systems. During this webinar, we will discuss the benefits, challenges and risks associated with going paperless. You will see how SharePoint can be used to automate validation projects through the use of electronic documents and templates, electronic workflows, and electronic signatures.
Among the topics included will be:
- Using integrated workspaces in SharePoint to manage validation documents
- Using workflows to manage validation document lifecycle and test execution
- Maintaining the validated state: Integration with change control and configuration management
- Automating traceability through the use of standards
- Leveraging business intelligence dashboards to manage validation projects
