Monitoring Impurities in Pharmaceutical Products - ICH Q3 requirements 2015 is a webinar that covers topics such as:
- Discuss warning letters and citations
- Understand regulatory expectations
- Review ICH Q3A for controlling impurities in API and Q3B for impurities in Drug Products
- Understand regulatory requirement guidelines surrounding impurities in API and Drug Products
- Understand different thresholds to report for regulatory submission
Monitoring Impurities in Pharmaceutical Products - ICH Q3 requirements 2015 brings together:
- QA and QC Managers
- R&D analysts
- Directors
- Regulatory scientists
- Regulators and Researchers who are responsible for providing analytical data pertaining to pharmaceutical products
