Analytical Method Validation for Pharmaceutical Quality Control 2018 is a seminar that covers topics such as:
- Validation terminology and experimental approaches to method validation
- Regulatory expectations for method validation/verification
- How to set meaningful acceptance criteria
- How to write effective test methods and validation protocols
- Strategies for dealing with validation failures
- The extent of method validation required at each stage of development
- How to set system suitability limits
Analytical Method Validation for Pharmaceutical Quality Control 2018 brings together:
- Quality Control Departments
- Quality Assurance Departments
- Analysts and Other Laboratory Staff
- Validation Specialists
- Regulatory Affairs Departments
- Lab Supervisors and Managers
- Research and Development Departments
- GLP/GCP/GMP Auditors
