In this webinar, we will review CAPA as part of Quality Management System (QMS), reasons why organizations need to use CAPA, what is its purpose. We will describe CAPA concepts and procedures. We will also describe FDA investigation procedure of CAPA.

Why should you Attend:
Corrective and preventive actions both include stages for investigation, action, review, and further action if required. Implementation of corrective and preventive actions is the path towards improvement and effectiveness of Quality Management Systems. Learn CAPA as part of Quality Management System (QMS), its purpose, its concepts and procedures. Learn how FDA investigates CAPA in organizations, and be prepared for an audit in your organization.

Areas Covered in the Session:
What is CAPA?
CAPA Concepts
CAPA Procedure

Who Will Benefit:
Quality Assurance
Documentation Managers
Records Managers
Document Control
Compliance
Medical Affairs

Speaker Profile:
Eleonora Babayants is a Galaxy Consulting Founder and President, She is a documentation management professional and hands-on consultant with over 25 years of experience in documentation and records management, document control, regulatory compliance, internal and external auditing, electronic document management systems, information governance, and change management.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

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