| Automated Validation Lifecycle Management – A Working Model - By Novartis & ValiMation |
| Description: |
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 |
| Location:
|
Web Seminar |
| Date: |
From:
9/23/2010To
9/23/2010 |
|
| Novartis, Microsoft, ValiMation present - Managing Validation Life Cycle Sans Paper: A Working Model |
| Description: |
This session 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. |
| Organizer:
|
DIA Annual Meeting |
| Location:
|
Washington DC |
| Date: |
From:
6/13/2010To
6/17/2010 |
|
| Automated Validation Lifecycle Management – A Working Model - By Novartis & ValiMation |
| Description: |
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 |
| Location:
|
Webinar |
| Date: |
From:
5/13/2010To
5/13/2010 |
|
| Paperless Training Management Webinars |
| Description: |
This web seminar presents an automated training management platform that eliminates paper completely.
Attendees will witness this paperless platform in action. |
| Organizer:
|
ValiMation abacusBPM |
| Location:
|
Webinars:
Register at: http://www.abacusbpm.com/csave_webinars.aspx |
| Date: |
From:
4/21/2010To
4/22/2010 |
|
| Paperless Validation Webinars |
| Description: |
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 resulting in large savings for the pharmaceutical / biotech / medical device industries.
|
| Organizer:
|
ValiMation abacusBPM |
| Location:
|
Webinars. Register at: http://www.abacusbpm.com/csave_webinars.aspx |
| Date: |
From:
4/13/2010To
4/15/2010 |
|
| Managing Cleaning Validation & Assessments Sans Paper - By Novartis and ValiMation |
| Description: |
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 |
| Location:
|
Webinar |
| Date: |
From:
10/21/2009To
10/21/2009 |
|
| Paperless Validation, A Case Study: Control Costs and Increase Efficiencies |
| Description: |
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 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.
During this event we will evlaute 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) |
| Location:
|
Webinar |
| Date: |
From:
8/5/2009To
8/5/2009 |
|
| Paperless Validation, A Case Study: Control Costs and Increase Efficiencies |
| Description: |
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 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.
During this event we will evlaute 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) |
| Location:
|
Webinar |
| Date: |
From:
6/30/2009To
6/30/2009 |
|
| PDA - Paperless Validation, A Case Study: Managing Validation Lifecycle Sans Paper - A Working Model |
| Description: |
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 |
| Location:
|
Webinar |
| Date: |
From:
5/21/2009To
5/21/2009 |
|
| PDA - Paperless Validation, A Case Study: Managing Validation Lifecycle Sans Paper - A Working Model |
| Description: |
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 |
| Location:
|
Webinar |
| Date: |
From:
3/12/2009To
3/12/2009 |
|
| GAMP 5 Industry Forum |
| Description: |
Integrating GAMP5 with Technology - Paperless Validation |
| Organizer:
|
SWE Enterprises |
| Location:
|
Tremont Marriott, Boston, MA |
| Date: |
From:
10/2/2008To
10/3/2008 |
|
| The Role of Business Process Management in FDA Regulated Industry |
| Description: |
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 |
| Organizer:
|
Barnett International |
| Location:
|
Webinar Dates: March 13, 2008; June 13, 2008. Contact: Margie@valimation.com |
| Date: |
From:
3/13/2008To
6/13/2008 |
|
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