CAPA Root Cause Analysis in 2016 by Compliance4all
- September 26, 2016
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The course takes one through the rigors of RCA as it applies to CAPA. There are ways of making the journey easier and structuring it so that the right answers are arrived at. This presentation presents highlights of a proper RCA, RCA tools and discusses dos and don'ts with regard to RCA.
Why should you Attend:
To learn the basics, understand what it is that the regulators are looking for. Establish a robust system for Root Cause Analysis. The course will cover the typical tools used in RCA as well how to present this information as part of the facility CAPA system.
Areas Covered in the Session:
Who Will Benefit:
Quality Systems Specialist
Those conducting RCA
Those managing the process
Louis Angelucci is a pharmaceutical professional and Certified Quality Engineer with over 20 years of experience in Quality Assurance, Quality Control, Validation, consent decree remediation as well as cGMP Compliance in the Medical Device and Pharmaceutical industries.
Compliance4All DBA NetZealous,
Event Link : http://bit.ly/2but5zV
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