Microsoft SharePoint is a powerful collaboration platform gaining more and more attention. If not already implemented in your company SharePoint most likely will be in the near future. Come explore the 3 scenarios of SharePoint implementation, and how to achieve the highest level of compliance in your organization. Partnering for this discussion will be QPharma, the industry's leading regulatory experts, and SOLABS, the creators of the easiest QMS to operate in the life science space.
If you are considering using SharePoint as a Document Control software and must deal with GxP requirements, you have several options. Explore 3 scenarios with us: 1. SharePoint alone 2. SharePoint & web parts 3. SharePoint & QMS software
Distinguished speaker:
Mr. Robert Finamore Director of Validation Services Robert J. Finamore serves as the Director of Validation Services for QPharma. He has been a leader at QPharma over the past 10 years in the management and execution of regulatory compliance projects, and is a recognized expert in computer system validation and 21 CFR Part 11 compliance. He currently oversees the professional services group, which executes regulatory compliance projects in the fields of validation, quality systems, medical device consulting, training, and auditing for life science clients. Robert holds a B.E. in Mechanical Engineering from Stevens Institute of Technology.
