Data integrity issues rarely begin with bad actors — they usually start with convenience.

In this episode, we examine how FDA auditors identify loss of system control through everyday practices like shared logins, manual entries without review, and backdating documentation. These shortcuts weaken compliance and raise serious red flags during inspections.

Learn how regulators evaluate whether systems can independently prevent, detect, and correct errors — and why robust design matters more than personal trust.

Topics covered:
• The real root causes of data integrity failures
• What auditors look for beyond data accuracy
• How weak controls compromise reliable records
• Designing systems that reduce human dependency
• Fixing documentation risks before inspection day

An essential episode for anyone responsible for GMP data and quality systems.

This episode presents Deviation and Root Cause Analysis through an unconventional lens: Mickey Mouse Clubhouse. By mapping cartoon problem-solving steps to pharmaceutical Quality practices, we discuss proper deviation documentation, risk assessment, investigation techniques, and CAPA effectiveness.

Ideal for:
• QA professionals
• Manufacturing and Engineering teams
• Students entering the pharmaceutical industry
• Anyone interested in building a strong Quality Culture