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.