This web seminar presents a platform that changes the status quo completely. The automated validation lifecycle management platform eliminates paper completely and changes the current paradigm. This platform increase efficiencies and thus while saving millions of dollars for the FDA regulated industry. Attendees will witness this paperless platform in action.
This session demonstrates that paperless validation is not an oxymoron. 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.
This web seminar presents a platform that changes the status quo completely. The automated validation lifecycle management platform eliminates paper completely and changes the current paradigm. This platform increase efficiencies and thus while saving millions of dollars for the FDA regulated industry.
This web seminar demonstrates Paperless Cleaning Validation and Assessments. This Paperless 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. Attendees will witness this paperless platform in action. 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.
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.
This web seminar demonstrates that Paperless Validation is not an oxymoron. A Paperless Validation plaftorm 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. Attendees will witness this paperless platform in action, which will surely become the mainstream. 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.
This web seminar describes Business Process Management (BPM) and its relevance to FDA regulated industry. This includes: Insight into the latest tools and technologies available to achieve efficiencies, compliance and automation of a variety of paper intensive business processes. Live demonstrations of some sample BPM solutions. Discussing technological solutions for real-life problems for the attendees
Conference Name
The Role of Business Process Management in FDA Regulated Industry
Organizer
Barnett International
Date
March 13, 2008; June 13, 2008; March 13, 2008; June 13, 2008; Sept 23, 2008; Dec 10, 2008
