2015 - Webinar On Robust Corrective And Preventive Action (CAPA)

Description : This 90 minute in-depth webinar will provide valuable assistance to all regulated companies that need to review and modify their company's CAPA system. Its principles apply to personnel / companies in the Medical Devices, Pharmaceutical, Diagnostic, and Biologics fields.
Areas Covered in the Session :
Regulatory "Hot Buttons"
CAPA Background
Correction, Corrective Action, Preventive Action Defined
Impact Analysis and Response - a Key Component
CAPA System Assessment
"Bullet-Proof"
Data Sources / Metrics
Monitor for Effectiveness
"Closed-Loop" - Lock In the Change
Beyond Regulatory Compliance
Who Will Benefit:
The employees who will benefit include:
Senior management
Middle management
R&D
Engineering
Software
QA / RA
Manufacturing
Operators
Consultants
cGMP instructors
And all personnel involved in verification and/or validation planning, execution and documentation