Understanding Corrective and Preventive Action, and Elements of a CAPA System - Webinar by GlobalCompliancePanel
September 2, 2010(Ended)
Online Webinar
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. This session will
discuss the importance, requirements, and elements of a CAPA program,
as well as describing the uses of CAPA data. Additionally, the
application of risk management to a CAPA program will be reviewed, and
a specific risk management system explained.
Areas Covered in the Session:- QSR and ISO 13485 requirements for CAPA
- Elements of a cross-procedural CAPA program
- Applications of CAPA
- CAPA data and its uses
- Application of risk management to CAPA program
- R&D management
- Regulatory management
- QA management
- Consultants
- Quality system auditors
Prices *
245 US Dollar (Early registration date: September 1, 2010)
Exhibition
No exhibition
Organization
Categories
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
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