Lifecycle Approach to Analytical Methods for Drug Products: Incorporating QbD Concepts into Method Development, Validation, Verification and Transfer 2017 is a seminar that covers topics such as:
- The different methods required for various drug products and the types of impurities which must be addressed
- The lifecycle approach to method development and validation
- Use an IQ/OQ/PQ approach to method qualification
- Identify an ATP for methods being developed
- Comply with compendial requirements with greater success and fewer resources
- Develop appropriate protocols for method transfer
Lifecycle Approach to Analytical Methods for Drug Products: Incorporating QbD Concepts into Method Development, Validation, Verification and Transfer 2017 brings together:
- Regulatory Affairs/CMC Personnel
- Chemists (Research, Quality Control, CRO)
- Analysts
- Laboratory Managers and Staff
- QA/QC Managers and Personnel