Discover Risk-Based Approaches for Qualifying SharePoint Enterprise Deployments and Validating SharePoint Composite Applications for FDA-Regulated Environments | Jan. 19, 2012, 2-3 PM EST | O’Driscoll/Youmans/Woergaard
July 15th, 2011 // 12:30 pm @ jmpickett
This Webinar by a team of seasoned GXP validation and SharePoint experts will introduce innovative best practice risk-based strategies, important processes and new exciting tools to help qualify enterprise Microsoft SharePoint deployments as well as validate mission critical applications such as clinical and investigator portals and document management in FDA regulated environments.
The presentation — by speakers Gerry O’Driscoll, US Data Management, Chris Youmans, InnovoCommerce, Martin Woergaard, EpistaIT — begins with a high level introduction to SharePoint enterprise planning and deployment considerations for life science organizations that will consider use of validated applications.
Note: All Expertbriefings.com Webinars are eligible for 1.0 CEU towards RACS Certification and 0.1 RU towards ASQ Certification.
Price: $349 ($50 Off Regular Price)
What You Will Learn:
•Understand strategic validation choices for the enterprise SharePoint farm(s).
•Understand GAMP 5 risk-based approaches to qualifying the enterprise SharePoint deployment–key strategic and tactical considerations.
•Learn a risk-based matrix approach to understanding, identifying and attributing risk factors for enterprise SharePoint farm deployments, configuration management and compliance monitoring and change control.
•Learn essential change control and configuration management strategies and associated set of processes to properly manage a SharePoint farm.
•Discover how innovative new tools can be used to monitor and manage the qualified SharePoint environment – automated tools have been introduced to track changes to SharePoint environments
•Learn from real-case scenarios that evidence the mission-critical importance of leveraging risk-based approaches to qualifying and managing SharePoint enterprise environments— whether they are validated or not.
Price: $349 ($50 Off Regular Price)
About the Speakers:
Gerry O’Driscoll, Vice President, Practice Development of Enterprise Content Management, US Data Management
Gerry O’Driscoll has over 15 years experience in enterprise software and services delivery in the pharmaceuticals, biotechnology, and medical device industries. His experience within the regulated technology industries is extensive. Gerry has worked for industry leaders such as Phase Forward, ClinPhone (Perceptive Informatics) and Qumas. During his industry tenure he has received recognition for business development achievements and management results.
Chris Youmans, Vice President, Operations, InnovoCommerce
Chris Youmans is a seasoned professional with over 18 years of management, architecture, development and consulting experience. Chris has over 10 years’ experience in the high technology sector and over 8 years’ experience in the biotech and pharmaceutical industry. Chris is a veteran of the US Navy where he served as an Explosive Ordinance Disposal Combat Diver and has a BS in Information Systems from National University. Prior to joining InnovoCommerce, Chris worked for Biogen Idec, Day Software (Recently purchased by Adobe) and Ernst & Young.
Martin Woergaard, Co-Founder of epistaIT
Martin Woergaard is the co-founder of epista IT, an independent Life Science Consultancy dedicated to helping its clients find the perfect balance between risk and compliance. We have deep roots in the Life Science industry which give us a comprehensive understanding of its regulatory requirements. And unlike most other Life Science consultants, we also have advanced knowledge of the relevant technology. The result? Solutions that lower compliance costs and improve business processes.
