All Upcoming Events

Overview of FDA Regulatory Compliance for Medical Devices
March 22 - 23, 2010
Dublin IRELAND
The Center for Professional Innovation and Education
info@cfpie.com
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Project Management for Phase 1 & 2 Clinical Trials
March 22 - 23, 2010
Malvern PA UNITED STATES
The Center for Professional Innovation and Education
info@cfpie.com
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Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
March 22 - 23, 2010
Costa Mesa CA UNITED STATES
The Center for Professional Innovation and Education
info@cfpie.com
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Pharmaceutical Production Batch Record Review
March 22 - 23, 2010
Costa Mesa CA UNITED STATES
The Center for Professional Innovation and Education
info@cfpie.com
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What are DHF, DMR and DHR? - The FDA Quality Systems Regulations Records Explained
March 22, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
admin@complianceonline.com
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Root Cause Analysis for CAPA
March 24 - 26, 2010
Dublin IRELAND
The Center for Professional Innovation and Education
info@cfpie.com
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Optimization of Drug-Like Properties in Drug Discovery - Assessment and Structure Modification Strategies
March 24 - 26, 2010
Costa Mesa CA UNITED STATES
The Center for Professional Innovation and Education
info@cfpie.com
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Project Management for Phast 3 & LCM (Life Cycle Management) of the Drug Development Process
March 24 - 25, 2010
Malvern PA UNITED STATES
The Center for Professional Innovation and Education
info@cfpie.com
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Overview of the Medical Device Risk Management Standard-ISO 14971
March 24, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
admin@complianceonline.com
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Clinical Evaluation Reports (CER's) Required for All Classes of Medical Devices in Europe
March 24, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
admin@complianceonline.com
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