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MEREDITH CRABTREE

GMP Auditing of Active Pharmaceutical Ingredients (APIs) and Excipient Suppliers

MEREDITH CRABTREE

November 20, 2023 | US Eastern Time: 10 AM to 4 PM | Central Europe Time: 4 PM to 10 PM

FDA/ICH Guideline Q9 (R1) On Quality Risk Management

MEREDITH CRABTREE

Duration: 90 Minutes

3-Hour Virtual Seminar On Root Cause Analysis, CAPA And Effectiveness Checks

MEREDITH CRABTREE

Duration: 3 Hour

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