FDA`s Update on Elemental Impurities According to the new ICH Q3D and USP 232/233 Guidelines - Are you ready? 2016 is a webinar that covers topics such as:
- Overview of Guidance Documents: FDA, ICH Q3D, USP 232/233
- Elemental Impurities: The case for Change
- Risk Assessment
- Scope of the guidances
- Controls and Documentation
- FDA Recommendations
- What you should be doing now
- Analytical Procedures and Validation
FDA`s Update on Elemental Impurities According to the new ICH Q3D and USP 232/233 Guidelines - Are you ready? 2016 is intended for:
- Regulatory Affairs personnel
- Pharmaceutical R&D and QC chemists and their managers
- Individuals at Contract Manufacturing and Contract Laboratory facilities
