Recorded: Access recorded version, only for one participant unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
Corporate Recorded: Access recorded version, Any number of participants unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
This webinar will provide a practical framework for identifying, analyzing, and addressing deviations in pharmaceutical and biopharmaceutical manufacturing.
Attendees will gain insights into regulatory expectations, key RCA methodologies such as the 5 Whys, Fishbone Diagram, and FMEA, and best practices for developing and implementing effective CAPA plans to prevent recurrence. The session will also cover common pitfalls in RCA and CAPA execution, real-world case studies, and strategies to ensure compliance with FDA, EMA, and ICH Q10 guidelines.
Participants will leave with actionable knowledge to enhance their investigation processes and strengthen their GMP compliance programs.
Why should you Attend:
Participants should attend this webinar to gain essential skills in conducting effective Root Cause Analysis (RCA) and implementing robust CAPA programs-key elements for ensuring GMP compliance and avoiding regulatory issues.
Designed for professionals in quality assurance, manufacturing, compliance, and regulatory affairs, this session provides practical tools, real-world case studies, and proven methodologies to help identify true root causes, prevent recurring issues, and enhance product quality and operational efficiency. With increasing regulatory scrutiny from FDA, EMA, and other global agencies, mastering RCA and CAPA is crucial for maintaining a proactive, risk-based approach to compliance. Take advantage of this opportunity to strengthen quality systems and improve overall regulatory readiness.
Areas Covered in the Session:
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