Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy (Oct 19 - 22, 2026)

Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy is organized by The Center for Professional Innovation & Education (CfPIE), Inc. and will be held from Oct 19 - 22, 2026.

Description:
Inadequate failure investigations continue to be a major GMP deficiency cited during routine and for-cause regulatory inspections. This course highlights FDA and EU regulations and how to successfully approach a failure investigation and engage in subsequent root cause analysis.

The primary objective of this course is to recognize the value of conducting proper root cause analysis and documenting failure investigations. Emphasis is placed on the application and practical, hands-on aspects of how to facilitate root cause analysis. Additionally, the course will provide attendees with the principles and techniques involved in identifying failures and deviations, categorizing problems, assigning responsibility and tracking team activities.

Additional benefits of this class include:

• Learn not just from the Director, but tap into the knowledge of your peers: Participants will have the opportunity to anonymously submit their challenges, problems, and issues for classroom discussion. Ample time is provided to address specific problems and questions of individual participants
• Explore the use of brainstorming, process mapping and regulatory resources
• Participants will also have the opportunity for one-on-one consultation with the Course Director during course breaks and in the evenings

Learning Objectives:
This course provides clarification of regulatory expectations and guidance, and the essential skills necessary to ensure effective and efficient investigations. Topics will examine each step of the investigation process from failure identification and notification through documentation. Participants will practice root cause analysis techniques and identify corrective and/or preventive actions towards successful remediation and closeout.

Attendees will gain a perspective of effective interviewing and writing skills, discuss common pitfalls, and develop tips and techniques for thorough investigations and elimination of recurring failures and deviations. Additionally, attendees will learn through hands-on activities such as group discussions and case studies tailored to regulated industries.