All too commonly, pharmaceutical manufacturers face quality systems challenges that cost time, money, and regulatory scrutiny. Learn more about the issues we most frequently see as we work with pharmaceutical innovators, generics manufacturers, and CDMOs worldwide. Most importantly, we’ll share strategies and tactics to strengthen your quality system.
Live Online Discussion
Tuesday, May 21, 2024
11:00 am ET / 9:00 PT
The discussion will include:
- Deviation, CAPA & change control management
- Common modality-specific pain points
- Quality system management for in-house, CDMO, and hybrid manufacturing constructs
- Strategies to reduce the number of deviations and to clear deviation backlogs
- Determining true root cause from contributing factors
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