Access our on-demand webinar that discusses proactive quality system management that allow pharmaceutical manufacturers to avoid time and resource-intensive filing approval delays, observations, and warning letters.
• 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
