Wednesday March 10, 2010 Wednesday March 10, 2010
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6th Annual Stability Testing Conference
Current Trends and Best Practices to Support Global Markets |
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The CTD and eCTD Formats for NDA & BLA SubmissionsMarch 23-24, 2010Philadelphia, USA
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Quality Risk ManagementMarch 30-31, 2010Somerset, NJ, USAWorkshops, Case Studies & Interactive Exercises
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Leadership WorkshopMarch 30-31, 2010Montreal, Canada
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Good Documentation Practices for GMP operations
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Process Validation for the 21st Century
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| TO BE ANNOUNCED... | |
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Investigating Out-of-Specification (OOS) Resultsfor Pharmaceutical, Biotechnology, Medical Devices and Allied Industries March 2-3, 2010Montreal, Canada |
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Pharmaceutical Microbiology & Best Practices
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Implementation of Effective & Compliant CAPA ProgramsApril 7-8, 2010Somerset, New Jersey
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Computer Systems Validation
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Cleaning Validation PracticesApril 14-15, 2010Montreal, Canada
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Project ManagementApril 14-15, 2010Montreal, Canada
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Designing Pharmaceutical GMP FacilitiesApril 20-21, 2010China
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Environmental Monitoring (EM) in Pharmaceutical ManufacturingApril 20-21, 2010New Jersey/New York
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Generic Drug Submissions and ApprovalApril 20-21, 2010New Jersey, USA
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Natural Health Products & Dietary SupplementsApril 21-22, 2010Montreal, Canada
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Residual Solvents Testing
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Aseptic Processing OperationsApril 26-27, 2010Philadelphia, PA
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Adverse Drug Event ReportsApril 27-28, 2010Europe
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Qualification & Validation of Facilities and UtilitiesApril 28-29, 2010Montreal -Canada
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HPLC Method Development & Validation Procedures
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Quality by DesignApril 28-29, 2010Europe
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FDA Pre-Approval InspectionsApril 28-29, 2010Montreal, Canada
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Technology Transfer Planning
for Pharmaceutical, Biopharmaceuticals, and Biotech |
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Global Regulatory Submissions ProcessTBA
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Third Party Audit & Supplier QualificationMay 4-5, 2010Philadelphia, PA
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Lyophilization Technology & System ManagementMay 4-5, 2010Philadelphia, PA
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Cleaning Validation PracticesMay 4-5, 2010Montreal, Canada
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Designing Pharmaceutical GMP FacilitiesMay 5-6, 2010Montreal, Canada
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Quality by DesignMay 5-6, 2010Montreal, Canada
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Fundamental Tools in Statistics for GMP ComplianceA Two-Day Case Studies & Workshops for Life Sciences Professionals May 10-11, 2010Prague, Czech Republic
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Investigating Out-of-Specification (OOS) Resultsfor Pharmaceutical, Biotechnology, Medical Devices and Allied Industries May 10-11, 2010Czech Republic
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Developing an Effective Complaint Handling and Recalls ProgramMay 12-13, 2010New Jersey, USA
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Analyzing Biological AssaysComputation, Validation, Acceptance & Troubleshooting May 12-13, 2010Toronto, Canada
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Pharmaceutical ImpuritiesAddressing US, European and ICH Requirements for Impurities; Strategies for Testing, Identifying and Controlling Impurities in Pharmaceuticals May 12-13, 2010Toronto, Canada
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Outsourcing Manufacturing and Partnerships with CMOsManagement Strategies to Develop Quality Partnerships in Pharmaceutical, Biopharmaceutical and Biotech Industries May 12-13, 2010New Jersey, USA
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Good Monitoring Practices for Medical DevicesMay 18-19, 2010Washington DC, USA
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Residual Solvents TestingMay 18-19, 2010Philadelphia, USA
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Generic Drug Submissions & ApprovalPreparing for Legal and Regulatory Requirements May 19-20, 2010Montreal, Canada
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Solid Dosage Production in cGMP ManufacturingPrinciples, Practices and Strategies May 19 – 20, 2010Jersey City, USA
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Productivity, Quality and Continuous Improvement with Lean Six SigmaMay 19-20, 2010Montreal, Canada
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Computer Systems ValidationMay 25-26, 2010United Kingdom
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Dissolution Testing in Pharmaceutical AnalysisMay 25 – 26, 2010Miami, FL - USA
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Technology Transfer PlanningPlanning and Management Strategies for a Successful Transfer for Pharmaceutical, Biopharmaceutical and Biotech May 26-27, 2010New Jersey, USA
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Design, Development, and Implementation of a Validation Master Plan (VMP)Best Practices for Managing Validation Activities May 26-27, 2010New Jersey, USA
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Cold Chain ManagementMay 26-27, 2010United Kingdom
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European Filing & RegistrationMay 26-27, 2010Europe
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Cleanroom & Contamination ControlJune 1-2, 2010Montreal, Canada
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Microbiological Food Safety ManagementJune 1-2, 2010Montreal, Canada
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Analytical Instrument & Equipment QualificationJune 2-3, 2010New Jersey, USA
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Process Analytical TechnologyJune 2-3, 2010New Jersey, USA
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Computer Systems ValidationJune 8-9, 2010Philadelphia, USA
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Regulatory Strategies for Natural Health ProductsJune 8-9, 2010Philadelphia, USA
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Effective SOP Development and Documentation ManagementJune 9-10, 2010Montreal, Canada
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Biologics ComparabilityJune 9-10, 2010Montreal, Canada
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Cleaning Validation PracticesFor Pharmaceuticals & Biotech Industries Production June 15-16, 2010Czech Republic
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Preparing & Implementing an Effective Change Control SystemJune 15-16, 2010Czech Republic
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Analyzing Biological AssaysComputation, Validation, Acceptance & Troubleshooting June 16-17, 2010Czech Republic
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How to prepare for System Based InspectionJune 16-17, 2010Europe
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Implementation of Effective & Compliant CAPA ProgramsWorkshops, Case Studies & Interactive Exercises June 23-24, 2010Toronto, Canada
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Effective Process ValidationJune 23-24, 2010Toronto, Canada
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Packaging and LabellingJune 23-24, 2010Toronto, Canada
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Cold Chain ManagementFor Pharmaceuticals & Biotech Industries Production June 29-30, 2010Philadelphia, USA
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Cleaning Validation PracticesFor Pharmaceuticals & Biotech Industries Production June 29-30, 2010Philadelphia, USA
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Residual Solvents Testing: How to Apply USP <467>Addressing US, European and ICH Requirements for Impurities; June 29-30, 2010Philadelphia, USA
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Preparing & Implementing an Effective Change Control SystemJune 29-30, 2010Montreal, Canada
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Preparation and Submission of Drug Master Files (DMFs)Strategy for Meeting Your Regulatory and Processing Responsibilities June 29-30, 2010Montreal, Canada
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Dissolution Testing in Pharmaceutical AnalysisJuly 14 – 15, 2010Budapest, Hungary
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Solid Dosage Production in cGMP ManufacturingJuly 20 – 21, 2010Calgary, Alberta
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GMP 2010Sept 28-29, 2010Toronto - CanadaA 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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Lab Expo - The Greatest Laboratory Event of 2010Oct 20-21, 2010Toronto - CanadaA 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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Cold Chain ManagementTBACanada
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