Practical HPLC Method Development & Validation

Venue: Hilton Montreal Airport

Location: Dorval, Montreal, Canada

Event Date/Time: Aug 23, 2007 End Date/Time: Aug 24, 2007
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Practical HPLC Method Development & Validation

Strategies for HPLC Method Development & Validation for Pharmaceutical APIs and Finished Products

With participation from Waters

A Two Day Interactive Training Seminar on:

- The cGMP regulations that govern the pharmaceutical laboratory
- Review ICH Q2 A&B guidelines for method development/validation
- Phase-appropriate method development and validation
- Forced degradation study designs to challenge the analytical methods
- Practical Separations for Biopharmaceuticals
- Modern Practice of Solid-Phase Extraction (SPE)
- Best Practices for Stability Testing in Pharmaceutical Development
- An overview of modern trends in HPLC columns and instruments
- HPLC Troubleshooting and Diagnostics
- How to be more successful and productive in HPLC
- Design you forced degradation studies to challenge the analytical methods
- Troubleshooting Strategies

Distinguished Course Leaders
Dr. Shib Mookherjea


12505 Cote de Liesse

Additional Information

Who Should Attend: This one & half day seminar and workshops is directed toward Directors, Managers, Supervisors, Analysts, and Associates in the Pharmaceutical, Biopharmaceutical, Biotechnology, and allied industries with responsibilities in the following areas: Quality Control Quality Assurance Quality Assessment Method Development Analytical Research Validation Process Development Product Testing R&D Manufacturing Regulatory Affairs Registration Fee: $795.00 + GST (6%) - Multiple Registrations: Send five attendees and the sixth is FREE!