Event Date/Time: May 16, 2006 End Date/Time: May 19, 2006
Registration Date: May 16, 2006
Early Registration Date: Mar 21, 2006
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Description

Major Concerns:
1. New USP chapters
2. Analytical Method Robustness
3. Performing Compliant OOS and OOT Result Laboratory Results
4. LC Method Development
5. Validating Bioanalytical Methods
6. Strategies for the Validation of Biotechnology Methods
7. Tools for Method Validation
8. Common Mistakes/Problems in Method Validation
9. HPLC Lifecycle Validation
10. Method Transfer
11. Validation Statistics
12. Outsourcing Method Validation
13. Process Analytical Technology (PAT)
14. Acceptance Criteria
15. Avoiding 483 warning letters

Venue

Charlemont Place
Dublin 2
Ireland
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