CAPA – The Heart of Your Quality System

Pre-Recorded CD Webinar
Approximately 90 minutes in length, Self Examination and Answer Key Included


Who Will Benefit
This training solution will benefit professionals in the following industries:

"Medical Device, Pharmaceutical, Human Tissue, Biotechnology”

In departments such as:

"QA/QC/RA, Manufacturing/Operations, Research and Development, Legal"

With job functions:

"Department managers and supervisors, QA/QC/RA specialists and engineers, Manufacturing and R&D engineers, chemists, scientists, formulators, documentation specialists, auditors, technicians"

CAPA systems have come under intense scrutiny by the FDA in recent years. This course will examine the current industry-FDA environment and will give you tools for survival; it will provide a step-by-step guide to the setting-up, operation, management and auditing of a CAPA system for today’s FDA regulated industry environment.

Section 1:

Background-Regulatory Requirements

Why do I need a CAPA System?

Why is CAPA the “Heart” of my Quality System?

Section 2:

What exactly is a CAPA System and what is it supposed to do?

What are the Essential Elements of an effective CAPA System?

Section 3:

How do I implement an effective CAPA System?

Why all these records; is there an easier way?

How can computer automation help?

CAPA – The Heart of Your Quality System

Order On-Line to Own This CD Webinar: $195.00