Thursday September 2, 2010 Thursday September 2, 2010
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Common Sense Computer Validation for Regulated SystemsSept 23-24, 2010Prague, Czech Republic
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GMP Update 2010Sept 28-29, 2010Montreal - Canada
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Combating Counterfeit DrugsToronto - Canada
Postponed to February 2011
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Drug safety and pharmacovigilance |
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Process Validation for Medical Devices |
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Pharmaceutical Packaging and Labeling |
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Pharmaceutical Water Systems |
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Stability and Specifications for Biological and Biotechnology Derived Products |
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Dissolution Testing in Pharmaceutical Analysis |
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Design and Implementation of Batch Recording SystemsOctober 5- 6, 2010Philadelphia, PA
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Analysis of Metal Impurities According to Proposed USP ChaptersOctober 5- 6, 2010Philadelphia, PA
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Advances and Efficiencies in Stability Testing
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CMC Regulatory ComplianceStrategy for Optimizing Your Chemistry, Manufacturing and Controls Program October 26 - 27, 2010Montreal, Canada
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Lab Expo - The Greatest Laboratory EventA Two-day Can't Be Missed Conference, Workshops, and Exhibition....... Combining Laboratory GMPs, Inspectional Issues, Method Development, Validation, and Stability Testing
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Pharmaceutical Regulatory Affairs |
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Pharmaceutical Impurities |
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Counterfeit Drugs |
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Technology Transfer Planning |
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Complaint Handling and Recalls Program |
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5th Annual Cold Chain & Logistics Management ConferenceNovember 2-3, 2010Somerset, NJ, USA
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Quality by Design (QBD) & Process Analytical Technology (PAT)Comprehensive and Practical Approaches to Effectively Applying Quality by Design System in Your Business & Adhering to Regulatory Requirements November 3-4, 2010Somerset, NJ, USA
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Implementation of Effective & Compliant CAPA ProgramsNovember 15 - 16, 2010San Diego, CA
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Combating Counterfeit MedicinesNovember 18-19, 2010Washington, DC
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The International API GMP Guidance:
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Good Laboratory PracticesIntroduction, Requirements and Tools for Implementation November 30 – December 1, 2010Montreal, Canada
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Food Safety Management |
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Implementing ICH Q8, Q9, Q10 |
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Technology Transfer for Bipharmaceutical |
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