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Posts tagged 21 CFR Part 11
Achieving Validation and Part 11 Compliance of Spreadsheets
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
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Implement 21 CFR Part 11 in the Pharmaceutical Stability Laboratory
Conference Name
Stability Testing Forum
Organizer
Center for Business Intelligence (CBI)
Location
Philadelphia, PA
Date
7/15/2004 To 7/16/2004
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21 CFR Part 11 and its Current Impact in the Pharmaceutical Stability Laboratory
Conference Name
Stability Testing Conference
Organizer
Barnett International
Location
Philadelphia, PA
Date
6/24/2004 To 6/25/2004
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Applying ISPE’s GAMP Guidelines to achieve 21 CFR Part 11 Compliance
Conference Name
Facilities Validation
Organizer
Barnett International
Location
Philadelphia, PA
Date
3/29/2004 To 3/30/2004
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Implement 21 CFR Part 11 in the Pharmaceutical Laboratory
Conference Name
Annual Rapid Methods In Microbiology
Organizer
Barnett International
Location
Philadelphia, PA
Date
1/29/2004 To 1/30/2004
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Developing, Implementing and Validating 21 CFR Part 11 Systems
Conference Name
Computer & Software Validation
Organizer
Barnett International
Location
Philadelphia, PA
Date
12/3/2003 To 12/5/2003
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Implement 21 CFR Part 11 in the Pharmaceutical Laboratory
Conference Name
Laboratory Equipment and Validation
Organizer
CBI (Center for Business Intelligence)
Location
Princeton, NJ
Date
9/29/2003 To 9/30/2003
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Developing, Implementing and Validating 21 CFR Part 11 Compliant Systems
Conference Name
GLP Compliance Strategies
Organizer
Barnett International
Location
Philadelphia, PA
Date
9/25/2003 To 9/26/2003
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Design and Validation of an Environmental Monitoring System with Part 11 Considerations
Conference Name
Stability Testing
Organizer
Barnett International
Location
Philadelphia, PA
Date
9/24/2003 To 9/25/2003
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Maximize Your Understanding of 21 CFR Part 11 Validation through an In Depth Analysis of the Requirements and Compliance Strategies
Conference Name
Compliance Strategies and Validation Requirements for HVAC Systems
Organizer
IIR
Location
Philadelphia, PA
Date
9/15/2003 To 9/16/2003
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