CAPA System and Uses of CAPA Data - 2017

MessageThis Webinar is over
Date Jun 19, 2017
Time 10:00 AM
Cost $150.00
Online
Overview:
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.

Areas Covered in the Session:
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

Who Will Benefit:
    QA management
    CAPA coordinator
    Regulatory Affairs management
    Executive management
    Consultants
    Quality System Auditors

Speaker Profile:
Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy and colonoscopy devices, where he oversees the operation of the quality system. In this position, Jeff is responsible for oversight of the document control system, including maintenance of regulatory documentation.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

 


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