Automated Validation Lifecycle Management – A Working Model - By Novartis & ValiMation

Webinar Topic

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.

Organizer

PDA

Date

9/23/2010

Novartis, Microsoft, ValiMation present - Managing Validation Life Cycle Sans Paper: A Working Model

Conference Topic

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.

Conference Name

DIA Annual Meeting

Organizer

DIA (Drug Information Association)

Location

Washington DC

Date

6/13/2010 To 6/17/2010

Automated Validation Lifecycle Management – A Working Model - By Novartis & ValiMation

Webinar Topic

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.

Organizer

PDA

Date

5/13/2010

Managing Cleaning Validation & Assessments Sans Paper - By Novartis and ValiMation

Webinar Topic

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.

Organizer

PDA

Date

10/21/2009

Paperless Validation, A Case Study: Control Costs and Increase Efficiencies

Webinar Topic

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.

Organizer

Institute of Validation Technology (IVT)

Date

6/30/2009; 8/5/2009

PDA - Paperless Validation, A Case Study: Managing Validation Lifecycle Sans Paper - A Working Model

Webinar Topic

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.

Organizer

PDA

Date

3/12/2009; 5/21/2009

This web seminar describes Business Process Management (BPM) and its relevance to FDA regulated industry

Topic

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