Analytical Method Validation Best Practices for Pharma Companies 2018 is an event dedicated to the various parameters required for a successful method validation.
Analytical Method Validation Best Practices for Pharma Companies 2018 covers topics such as:
- Reasons for validation
- Selectivity – do this first
- Protocol or SOP
- Precision
- Linearity
- Ruggedness
- Sensitivity
- Inter-analyst variability
Analytical Method Validation Best Practices for Pharma Companies 2018 intended for:
- 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
