Analytical Method Validation Best Practices for Pharma Companies 2018

Analytical Method Validation Best Practices for Pharma Companies 2018 is an event dedicated to the various parameters required for a successful method validation.

Topics

• Reasons for validation
• Selectivity – do this first
• Protocol or SOP
• Precision
• Linearity
• Ruggedness
• Sensitivity
• Inter-analyst variability

Who should Attend

• Analytical Chemists responsible for Method Validation
• Those responsible for hosting FDA inspections, responding to 483s and Warning Letters
• Supervisors and Managers of Analytical Chemists
• Regulatory Affairs or those preparing NDAs or ANDAs