GlobalCompliancePanel to organize - “Root Cause Analysis and Documentation Requirements for CAPA”
12/04/2012

“Root Cause Analysis and Documentation Requirements for CAPA” is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on December 6.

Online PR News – 04-December-2012 – Online Training – Description:
This webinar explains the elements of Root Cause Analysis and Documentation Requirements for CAPA.
Root Cause Analysis (RCA) is undoubtedly the most potent tool in problem solving, since, as its nomenclature suggests, it gets to the root or source of the problem. But in real life, it is not as easy as it sounds, because there are too many variable and subjective factors at work. If making the RCA were simple, problem would not recur, as they almost always do.
The fundamental problem starts with defining the root cause. Many causes appear to be root causes, but they may not be soin reality. This webinar will be a humorous and lively elucidation of how to distinguish between a real root cause and a phony one. Attendees of this webinar will be able to distinguish between the ‘real’ and ‘fake’ RCA while working on it to implement their CAPA.
This webinar will teach participants to see RCA in relation to the system interactions and cultural environment in which it is made. This is very important because these are what usually lie at the root of a Root Cause Analysis, and often come in the way of arriving at an RCA.
-----------------------------------------------------------------------------------------------------------------
When:December 6, 10:00 AM PDT | 01:00 PM EDT
-----------------------------------------------------------------------------------------------------------------
By whom:

Anthony DeMarinis is Quality Systems Manager at Sealed Air.

Tony has BS degrees in Biology and Microbiology and an MS in Quality Management. He is currently Quality Manager at Sealed Air, a supplier of rigid medical device packaging solutions. Previously, he was Quality Systems Manager at Davol, Director of Quality Assurance at Scott Laboratories and Sr. Microbiologist at the National Cancer Institute.

He is a Certified Quality Auditor-BioMedical and Certified Manager of Quality and Organizational Excellence by the American Society for Quality. Tony also loves to teach. He teaches refresher courses for these certification programs through the local RI-ASQ section.

For over two decades, Tony has worked with using quality management techniques and value added auditing, which has included the use of Failure Investigation and Root Cause Analysis to improve processes and products.
-----------------------------------------------------------------------------------------------------------------
For whom:
The webinar will benefit
o QA and Manufacturing Managers
o Engineers
o Supervisors
o Consultants
o Auditors
o Executives or other individuals responsible for managing the CAPA system and resolving problems in any organization
----------------------------------------------------------------------------------------------------------------
Duration: 60 minutes
-----------------------------------------------------------------------------------------------------------------
To enroll for this webinar, contact
webinars@globalcompliancepanel.com
Phone: 800-447-9407