Mar. 01 - 03, 2010
 Biostatistics for Non-Statisticians
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Mar. 03 - 05, 2010
The Drug Development Process - From Discovery to Commercialization
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Mar. 08 - 10, 2010
Good Clinical Practices (GCPs)
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Mar. 15 & 16, 2010
Validation of Computer Systems
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Apr. 12 - 14, 2010
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
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Apr. 12 & 13, 2010
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
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Apr. 14 - 16, 2010
CMC Regulatory Compliance for Biopharmaceuticals and Biologics
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Apr. 15 & 16, 2010
Writing Effective Standard Operating Procedures and Other Process Documents
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Apr. 19 - 21, 2010
QA/QC Strategy for Biologics and Biopharmaceuticals
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Apr. 19 & 20, 2010
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
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Apr. 22 & 23, 2010
Introduction to Effective Medical Writing
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Apr. 22 & 23, 2010
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
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Apr. 26 & 27, 2010
The EU Clinical Trial Directive
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Apr. 28 & 29, 2010
European Filing & Registration Procedures
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May 17 & 18, 2010
Practical Methods for Project Management
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May 19 - 21, 2010
Root Cause Analysis for CAPA
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May 24 & 25, 2010
Clinical Trial Design For Medical Devices
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May 24 & 25, 2010
Overview Of FDA Regulatory Compliance For Medical Devices
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May 26 - 28, 2010
Process Validation for Medical Devices
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