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33842 Conferences

Root Cause Analysis and Documentation Requirements for CAPA - Webinar By GlobalCompliancePanel

Added by globalcompliancepanel on 2012-11-13

Conference Dates:

Start Date Start Date: 2012-12-06
Last Date Last Day: 2012-12-06

Conference Contact Info:

Contact Person Contact Person: John Robinson
Email Email: globalcompliancepanel@gmail.com
Address Address: 1000 N West Street | Suite 1200, Wilmington, Delaware, 19801, United States
Phone Tel: 800-447-9407
Phone Fax: 302-288-6884

Conference Description:

Overview: RCA is a popular topic and many companies realize its importance in correcting problems. However, there is still much confusion and many problems continue to recur. This webinar will use thoughtful discussion, humorous analogies and case studies to distinguish between the true root cause and other common imposters. Emphasis will be placed on realizing system interactions and cultural environment that often lies at the root of the problem and prevents true root cause analysis.

Areas Covered in the Session:
How the organizational culture and environment encourages problems
Role of Management and system interactions in causing problems
Root Cause Analysis Methods & Practical Applications
Case study examples to distinguish between assignable causes, enabling factors and root causes
System Thinking: Moving from a reactive to a proactive environment
Solution Development and Error Proofing
Documentation Requirements

Who Will Benefit: This discussion will provide individuals with the necessary tools to understand problems and prevent them from recurring and should be of interest to:
QA and Manufacturing Managers
Engineers
Supervisors
Consultants
Auditors

Executives or other individuals responsible for managing the CAPA system and resolving problems in any organization
Tony has BS degrees in Biology & Microbiology and a 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. He also teaches the refresher courses for these certification programs through the local RI-ASQ section. Tony has over 20 years experience using quality management techniques and value added auditing including the use of Failure Investigation and Root Cause Analysis to improve processes and products


GlobalCompliancePanel
Phone: 800-447-9407
Fax: 302-288-6884

webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com
1000 N West Street | Suite 1200 | Wilmington | DE | USA | 19801
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