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2011 PDA Visual Inspection Forum
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NEW! PDA Post-Conference Training Course: Development of a Freeze Drying Process
Interest Group Meeting Pre-filled Syringes
NEW! PDA Training Course: Contract Manufacturing in the Pharmaceutical Industry: From Start-Up to Market Supply
Contract Manufacturing in the Pharmaceutical Industry: From Start-Up to Market Supply
Workshop on Near IR - Manufacturing Uses & Recent Regulatory Guidance
2010 Pharmaceutical Freeze Drying Technology: Modern Trends in Production
PDA Workshop on Analytical Method and Procedure Validation: - An In-depth Review of the Global Requirements Governing Test Method and Procedure Development and Validation
PDA Training Course: An Introduction to Visual Inspection
PDA Presents a Series of Biopharmaceutical Events in Europe!
2010 PDA Europe Conference: Modern Biopharmaceutical Manufacturing – Current Best Practice
PDA Europe Workshop on Lean Manufacturing
NEW! PDA Training Course: Good Distribution Practice
Parenterals 2010: Integrating Process, Technology and Regulation
ICH Quality Implementation Working Group (Q-IWG) Integrated Implementation Training Workshops for ICH Q8, Q9 and Q10
2010 PDA Europe Visual Inspection Forum
2010 PDA Europe Workshop on Filtration
2010 PDA Europe Conference on Pharmaceutical Cold Chain Management
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PDA Workshop on Technical Report 22: Process Simulation Testing for Aseptically Filled Products
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Interest Group Meeting: Pre-filled Syringes
PDA Hands-on Workshop on Disposables/Single-Use-Technology
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2009 PDA Europe Conference on Endotoxins
PDA Workshop on Annex 1 EU GMP Guide and Its Impact on Media Fill Practices
Global Challenges for Investigational Medicinal Products
PDA Discussion Forum on Revision of Annex 1 to the EU GMP Guide: Issues and Challenges
Monoclonal Antibodies: Trends in Science, Technology and European Regulatory Considerations
Sterilisation Technologies in Development and Manufacturing of Parenterals
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Process Validation for Pharmaceuticals – Current and Future Trends
CGMP Training for Sterile Manufacturing
Strategies for Reducing Human Error Nonconformances – New Course
Effective Application of a Quality Systems Approach to Pharmaceutical CGMPs in Compliance with the FDA Guidance
Biotechnology: Overview of Principles, Tools, Processes and Products
Clean Room Design, Contamination Control, and Environmental Monitoring for Controlled Environments
2011 PDA Annual Meeting Course Series
Raw Materials “Ins and Outs” in the Pharma Arena – New Course
Risk Management in Aseptic Processing
Solving Strategic Quality, Regulatory and Technical Issues During the Development of Prefilled Syringes, Autoinjectors and Injection Pens
Global Regulations and Standards: Influences on Cold Chain Distribution, Packaging Testing and Transport Systems
Root Cause Investigation for CAPA
Risk Mitigation Solutions: The Response to Risk Assessment
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Practical USP Microbiological Test Methods
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Developing the Regulatory Rationale for the Reduction of Environmental and Utility Testing within an Environmental Monitoring Program
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Computer Product Supplier Auditing Process Model: Auditor Training
Basic Microbiology for Aseptic Processes
2010 PDA/FDA Joint Regulatory Conference Course Series
Fundamentals of Lyophilization
Bioassay Development and Validation
Achieving cGMP Compliance During Development of a Biotechnology Product
Integration of Risk Management into Quality Systems – Expanded
2010 PDA/FDA Vaccine Conference Course Series
2010 New Brunswick Course Series
Elements of Risk Management
2010 Universe of Pre-Filled Syringes and Injection Devices - TRI Course Series
PDA's 5th Annual Global Conference on Pharmaceutical Microbiology Course Series
Choosing the "Right" Microbial Identification Program for Your Biopharmaceutical/Pharmaceutical Quality Control Laboratory
2010 San Diego Course Series
Global Regulations and Standards: Influences on Cold Chain Distribution, Packaging Testing and Transport Systems
2010 PDA Annual Meeting Course Series
2010 Aseptic Processing Training Program
2009 PDA/FDA Joint Regulatory Conference Course Series
Downstream Processing: Separations, Purifications and Virus Removal
Development of Pre-filled Syringes
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Safety Ventilation in Biotech and Pharmaceutical Cleanrooms; Risk Assessment of Airborne Contamination
Fundamentals of D, F, and z Value Analysis
Validating a Steam Sterilizer
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An Introduction to Visual Inspection
Sterile Filtration in the Biopharmaceutical Industry, Course II
Contamination Control
Application of Disposables in Biopharmaceutics
Effective Application of a Quality Systems Approach to Pharmaceutical cGMPs in Compliance with the FDA Guidance
Methods Validation
Developing a Moist Heat Sterilization Program within FDA Requirements
Cleaning Validation
Environmental Mycology Identification Workshop
Developing an Environmental Monitoring Program
Global Regulations and Standards: Influences on Cold Chain Distribution, Packaging Testing and Transport Systems
2010 Boston Course Series
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2011 Aseptic Processing Training Program
Critical Utilities for Parenteral Manufacturing - New Course
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Validation of Moist Heat Sterilization Processes: Cycle Design, Development, Qualification and Ongoing Control
PDA Canada Chapter 2008 Fall Dinner Conference, Quebec City
PDA Canada Chapter 2008 Fall Dinner Conference, Montreal
Training Workshop on PDA Technical Report No.1, Revised 2007
Training Workshop on PDA Technical Report No. 26, Revised 2008
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2009 PDA Annual Meeting: Exhibition and Sponsorships
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PDA’s 3rd Annual Global Conference on Pharmaceutical Microbiology
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