All Upcoming Events

Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
March 17 - 19, 2010
Malvern PA UNITED STATES
The Center for Professional Innovation and Education
info@cfpie.com
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Sterilization Procedures: Technology, Equipment & Validation
March 17 - 18, 2010
Malvern PA UNITED STATES
The Center for Professional Innovation and Education
info@cfpie.com
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Purchasing Controls in the Medical Device Industry
March 17 - 18, 2010
Malvern PA UNITED STATES
The Center for Professional Innovation and Education
info@cfpie.com
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Preparing for FDA GLP Audits
March 17, 2010
Live Webinar PQ CANADA
BenAstrum
ardy.heydari@benastrum.com
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Design Validation Protocol and Acceptance Criteria for Chromatographic Methods to meet ICH requirements
March 17, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
admin@complianceonline.com
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Out-of-Specification Investigations – Beyond the laboratory
March 18, 2010
Palo Alto CA UNITED STATES
ComplianceOnline
admin@complianceonline.com
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Developing an Environmental Plan for a Controlled/Classified Environment
March 18, 2010
Live Webinar PQ CANADA
BenAstrum
ardy.heydari@benastrum.com
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Asthma and COPD: Clinical Drug Development
March 22 - 23, 2010
Arlington VA UNITED STATES
PERI, Inc
registrar@peri.org
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microRNA in Human Disease & Development
March 22 - 24, 2010
Cambridge MA UNITED STATES
CHI
chi@healthtech.com
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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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