All Upcoming Events

ComplianceOnline Webinar - How to conduct a software risk assessment that is meaningful
September 7, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
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ComplianceOnline Webinar - How do I keep FDA happy with my contract manufacturer?
September 8, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
admin@complianceonline.com
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ComplianceOnline Webinar - Engineering and Laboratory Mythology with Water System
September 8, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
admin@complianceonline.com
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Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
September 8 - 10, 2010
Costa Mesa CA UNITED STATES
The Center for Professional Innovation & Education
info@cfpie.com
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Introduction to Molecular Biology Techniques
September 8 - 10, 2010
King of Prussia CA UNITED STATES
The Center for Professional Innovation & Education
info@cfpie.com
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Preparing the CMC Section for NDAs/CTDs/INDs
September 9 - 10, 2010
Costa Mesa CA UNITED STATES
The Center for Professional Innovation & Education
info@cfpie.com
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Controlling Change to meet GMP Requirements
September 9, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
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ComplianceOnline Webinar -Developing Supplier Quality Auditor Training Programs
September 9, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
admin@complianceonline.com
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ComplianceOnline Webinar - Key Factors to Write an Effective Standard Operating Procedure (SOP)
September 9, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
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ComplianceOnline Webinar - Configuring Your System for Lean Documents
September 10, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
admin@complianceonline.com
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