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2017 - Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data



Venue2754 80th Avenue, New Hyde Park, NY 11040, USA - United States USA - United States

KeywordsExamples of capa in pharmaceut; Fda capa training; Root cause analysis training


Topics/Call fo Papers

Year after year, CAPA is the subsystem cited most frequently during FDA inspections. A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer. A system that identifies and eliminates nonconformances and potential nonconformances enables both regulatory compliance and cost savings.
Why Should You Attend
This webinar will identify the most common elements identified as deficient by FDA, and provide recommendations for how to provide clear, concise documentation to assure FDA your firm has addressed these in your quality system. This webinar also provides recommended forms to assure that in addition to being able to illustrate compliance; your firm’s CAPA system is useful and meaningful.
Areas Covered in this Webinar
Regulatory Requirements
ISO 13485
Elements of a cross-procedural CAPA program
Applications of CAPA
CAPA Data and best practices for its use
Application of risk management to CAPA program
For more detail please click on this below link:
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Last modified: 2017-04-21 20:42:44