Sep. 16 & 17, 2010
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
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Sep. 20 - 22, 2010
CMC Regulatory Compliance for Biopharmaceuticals and Biologics
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Sep. 20 & 21, 2010
Validation of Computer Systems
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Sep. 22 - 24, 2010
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
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Sep. 27 & 28, 2010
Adverse Drug Events – Reporting & Regulatory Requirements
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Sep. 27 & 28, 2010
Design Control for Medical Device Professionals
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Sep. 27 & 28, 2010
Writing Effective Standard Operating Procedures and Other Process Documents
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Sep. 29 - Oct. 1, 2010
The Drug Development Process - From Discovery to Commercialization
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Sep. 29 & 30, 2010
Design Validation, Verification, and Risk Analysis for Medical Device Professionals
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Sep. 30 & Oct. 01, 2010
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
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Oct. 05 & 06, 2010
The EU Clinical Trial Directive
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Oct. 07 & 08, 2010
European Filing & Registration Procedures
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Oct. 11 & 12, 2010
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
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