Summarize best practices for audit preparation, execution, and follow-up, integrating lessons from recent case studies and industry trends. Comprehend the CAPA process, risk management strategies, and emerging regulatory expectations that shape audit outcomes. Understand the importance of data integrity, GMP, and risk management to produce higher-quality products.

The main point of audit readiness is to emphasize a proactive approach to ensure that manufacturing operations remain robust, transparent, and compliant with current cGMP standards. Mock inspections, continuous process improvement, and thorough documentation are all key components of a quality program. Look at strategies to address any concerns, follow through on FDA investigations, and avoid getting an OAI classification to ensure that all products are made safely and follow all guidelines.