Conferences
- 21 CFR Part 11
- Accretive Model
- Automated Validation Lifecycle Management
- Batch Records
- Building Automation
- Business Process Automation (BPM)
- Case Study
- Change Control
- Cleaning Validation
- Clinical
- Control Systems
- Data Archiving
- Data Management
- eClinical Trials
- Electronic Records
- Electronic Signatures
- Enterprise Backup System
- Environmental Monitoring
- ERP
- FDA
- GAMP
- IT Compliance
- IT Infrastructure
- Java
- Lab Automation
- Master Validation Planning
- Network Qualification
- Paperless Validation
- Presentation
- Process Analytical Technology (PAT)
- Process Automation
- QBD
- Risk Based Validation
- SDLC
- Software Development
- Spreadsheets
- Test Automation
- Validation
Featured
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
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
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
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
Conference Name
GAMP 5 Industry Forum
Organizer
SWE Enterprises
Location
Boston, MA
Date
10/2/2008 To 10/3/2008
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
Conference Name
4th Annual Laboratory Instrument Qualification and System Validation Conference
Organizer
SWE, Inc.
Location
Boston, MA
Date
8/17/2007 To 8/18/2007
Conference Name
Third Annual Advanced Computer System Validation
Organizer
SWE Inc.
Location
Boston, MA
Date
5/17/2007 To 5/18/2007
Conference Name
eClinical Trials & Data Management
Organizer
Barnett International
Location
Course Dates and Locations: May 7, Philadelphia, PA; Sept 24 Philadelphia, PA; Nov 13 Philadelphia, PA
Date
2/12/2007 To 11/13/2007
Conference Name
SCDM 2006 Fall Conference
Organizer
SCDM
Location
Lake Buena Vista, FL
Date
10/8/2006 To 10/11/2006
Conference Name
eClinical Trials & Data Management
Organizer
Barnett International
Location
Course Dates and Locations: Sept 18, Philadelphia, PA; Nov 3, Philadelphia, PA
Date
9/18/2006 To 11/3/2006
Conference Name
PDA Annual Meeting
Organizer
PDA (Parenteral Drug Association)
Location
Anaheim, CA
Date
4/24/2006 To 4/28/2006
Conference Name
21st Annual DIA Clinical Data Management Symposium & Exhibition
Organizer
DIA
Location
Philadelphia, PA
Date
3/26/2006 To 3/29/2006
Conference Name
Interphex 2006
Organizer
Interphex
Location
Jacob Javitz Center, New York City
Date
3/23/2006 To 3/23/2006
Conference Name
IT Infrastructure Qualification Summit 2006
Organizer
Pharma IQ (IQPC)
Location
San Diego, CA
Date
2/27/2006 To 3/2/2006
Conference Name
Implementation & Benefits of a Disaster Recovery Business Continuity Program
Organizer
SWE Inc.
Location
San Diego, CA
Date
1/30/2006 To 1/31/2006
Conference Name
Techniques and Strategies for Advanced Computer System Validation
Organizer
SWE Enterprises
Location
Whippany, NJ
Date
10/13/2005 To 10/14/2005
Conference Name
eClinical Trials & Data Management
Organizer
Barnett International
Location
Course Dates & Locations: Feb 12 -13, Philadelphia, PA; Mar 30 - 31, San Deigo, CA; May 15 - 16, Edison, NJ.
Date
9/8/2005 To 5/16/2006
Conference Name
The Impact and Benefits of Process Analytical Technology
Organizer
SWE Enterprises
Location
Whippany, NJ
Date
6/16/2005 To 6/17/2005
Conference Name
Laboratory Instrument Qualification and Systems Validation
Organizer
SWE Enterprises
Location
Whippany, NJ
Date
5/2/2005 To 5/3/2005
Conference Name
Interphex Conference 2005
Organizer
Interphex
Location
Javits Convention Center, NY
Date
4/26/2005 To 4/28/2005
Conference Name
Lab Equipment Validation and Qualification
Organizer
Barnett International
Location
Philadelphia, PA
Date
3/7/2005 To 3/8/2005
Conference Name
Achieving Infrastructure and IT Compliance Conference
Organizer
SWE Enterprises, Inc.
Location
La Jolla, CA
Date
1/31/2005 To 2/1/2005
Conference Name
The Impact and Benefits of Process Analytical Technology
Organizer
SWE Enterprises
Location
La Jolla, CA
Date
1/31/2005 To 2/1/2005
Course Description
Computer Validation for the 21st Century – A 2 Day Seminar By ValiMation. This course will show attendees how to design a computer validation program to meet today’s networked and highly integrated GxP environment.
Conference Name
Computer Validation Course
Organizer
Barnett International
Location
Course Dates & Locations: Mar 29-30, San Francisco, CA; May 16-17 Raleigh, NC; June 13-14, San Francisco; Aug 29-30, Philadelphia, PA; Sept 22-23, San Francisco, CA; Nov 17-18, Boston, MA.
Date
1/1/2005 To 11/18/2005
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