Quality Matters Series: Thwarting Nonconformity: CAPA vs. Preventive Action

Have you ever read an article and wished you could speak directly with its author to learn more about the subject?  AAMI is making that concept a reality.  Take advantage of this unique opportunity to listen to a follow-up presentation with the author of the Quality Matters column featured in AAMI’s journal, Biomedical Instrumentation & Technology (BI&T).

The Quality Matters column is written with quality assurance and regulatory affairs professionals in mind and covers topics ranging from process validation and risk management processes to combination products and FDA inspections.

PROGRAM OVERVIEW
The third webinar in the Quality Matters Series explains the differences between CAPA and preventive action, how monitoring activities are used to determine whether a nonconformity has occurred, and how to characterize nonconformities to determine if a mandatory or voluntary action is required.  At the conclusion of the program, you come away with an understanding of how implementing a strong preventive action process at your organization will ensure that both your business and quality objectives will be achieved more consistently and effectively.

SPEAKER

WEBINAR CD

THREE WAYS TO PURCHASE

1. Phone – 1-877-249-8226 or 240-646-7031 to order with a credit card
2. Fax – Select and download the order form and fax to 240-396-5781 .
3. Mail – Select and download the order form and mail with payment to:

CAPA Webinar CD Package
AAMI Publications
PO Box 0211
Annapolis Junction, MD 20701-0211

QUESTIONS?
For questions about ordering the CD, please contact AAMI's Publications at 1-877-249-8226 / 240-646-7031. For content questions, please contact Jeanine Beisel at 703-525-4890, ext. 1212.