Paperless Validation, A Case Study: Control Costs and Increase Efficiencies
This web seminar demonstrates that Paperless Validation is not an oxymoron. The current fiscal state of the pharma industry coupled with FDA’s Quality By Design (QBD) initiatives makes it inevitable for the status quo to take the typewriter route. A Paperless Validation platform leverages web 2.0 technology to change the current paradigm. This platform can increase efficiencies while saving millions of dollars for the FDA regulated industry. During this event we will evaluate all phases of the validation process including; document template management, document authoring, protocol executions and project management while leveraging Microsoft’s .NET™ platform to eliminate paper completely.