COURSE ID 2089

How to Conduct Robust Root Cause Investigations for CAPA

AVAILABLE ON-DEMAND
Duration: 8 Hours
Course Instructor

Louis Angelucci

Price
$ 1560
Discounts: We offer a 10% group discount when you register 2 or more attendees (up to 10). Contact us for groups over 10.

Course description

View Course Outline

One of the most common FDA 483 and Warning Letter citations continues to be inadequate investigations. The FDA uses investigation reports and investigation trends to identify potential quality problems in all areas of the company. Ultimately, inadequate investigations can lead to 483 citations, Warning Letters, release of a sub-standard product, or product recall. Furthermore, costly and time-consuming system remediation may be required.

Having a procedure for Deviation Investigations is not enough. It is the content and conclusions of the investigations themselves that truly count. Doing a proper root cause analysis, gathering evidence, and ensuring a sustainable corrective action is key to a proper deviation investigation.

This accredited training will help attendees understand the fundamental investigation steps and skill sets. Key focus will be placed on identification and initial reporting of deviations, fact/evidence gathering, and arriving at the correct root cause and CAPA. The importance of investigation planning, critical thinking skills, and effective preventative action plans will also be discussed.

Root Cause Analysis (RCA) is an important technique practiced by many successful companies. It is used to determine the Corrective Action and Preventive Action CAPA procedures that are mandatory for the Quality Management Systems (QMS).

This training improves the way you analyze, document, and verify the root causes of a problem so that you can prevent its recurrence. This course will also include discussions on proper CAPA system maintenance, documentation of the Corrective and Preventative Actions, and developing a robust CAPA plan. It will give tips on how to develop CAPAs pertaining to longer-term projects and ensure they stay on track.

Upon completion of this course, you will be able to:

  • Outline the requirements of the Deviation and procedure including the deviation report
  • Choose the most appropriate Root Cause Analysis methods for the situation
  • Discuss how to conduct the deviation and the tools to be use… 
  • Review and discuss an example deviation using the tools suggested
  • Outline the requirements of the CAPA process and procedure including building a CAPA file
  • Establishing a CAPA plan: project summary, individual responsibilities and expected completion dates
  • Managing and Overseeing of the CAPA system and its documentation

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This is an informative and interactive seminar for professionals in the pharmaceutical, biological, and medical device industries who conduct deviations, Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) investigations, especially for professionals in the following disciplines:

  • Quality Control Analysts
  • R&D
  • Quality Assurance
  • Manufacturing
  • Product/Process Development
  • Engineering

Course Instructor

Louis-Angelucci

Louis Angelucci

Consultant for the Pharmaceutical Industry

Louis Angelucci’s Courses

Accreditation

Team Training

When you need on-site attention, we’re not just here to help, we’re there to help—right by your side.

Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.

In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.

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