2018 - Why Organizations need to use CAPA, What is its Purpose?
Date2018-06-07
Deadline2018-06-05
VenueFremont, USA - United States
KeywordsRecords Managers; Medical Affairs; Quality Assurance
Topics/Call fo Papers
Overview:
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: support-AT-compliance4All.com
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: support-AT-compliance4All.com
Other CFPs
Last modified: 2018-04-20 15:50:33