Description
<strong>Course Schedule - April 15-16, 2009</strong><br/><br/>Most organizations have procedures for implementing
corrective and preventive actions, but many do not have an
effective methodology to actually investigate to find the root
cause. As a result the investigation is often careless,
unsuccessful, and costly. Root Cause Investigation for CAPA
is a proven methodology to investigate and identify the root
cause when there has been a shift in the performance of a
product, machine, equipment, work process or system.
The methodology identifies the change (or changes) that
has occurred so that the change can be eliminated and the
performance can return to its previous level. It is ideal for
investigating an increase in:<br><br>
• Product or service defect levels<br>
• Customer complaints<br>
• Negative patient reactions with the product<br>
• Manufacturing scrap or rework<br>
• Equipment or process aberrations<br>
• Any performance change where a CAPA investigation is<br> required<br><br>
In this exciting and team-based seminar you will be challenged
to apply the methodology and tools on real case studies. This
will prepare you to confidently conduct successful
investigations immediately upon returning to work.
01/13/2009
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Medical Device
Course Category
Brochure Name
http://www.cfpa.com/PDF/2009/2089,C8-201,0904-301.pdf
Address
Burlingame, CA USA