Death by CAPA - Does your CAPA Program need a CAPA?

Website http://www.globalcompliancepanel.com/seminar/CAPA-program-need-a-CAPA-Philadelphia-901972SEMINAR?our | Edit Freely

Category Educational trainings, HR professionals, Human Resource, Online trainings, Employee Relations

Deadline: October 22, 2019 | Date: October 24, 2019-October 25, 2019

Venue/Country: Philadelphia, PA, U.S.A

Updated: 2019-08-16 16:18:52 (GMT+9)

Call For Papers - CFP

We'll discuss regulatory requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls. We'll discuss best practices so you can start off on the right foot and always be prepared for an inspection.

This seminar will provide detailed lectures on all elements of a CAPA program and how they connect to other parts of your Quality Management System. You will learn how to create a CAPA program that results in improved product quality, reduction in compliance issues, and ultimately leads to improved business success.

Why you should attend:

Corrective and Preventive Action (CAPA) is the cornerstone of a strong Quality Management System. And yet, many medical device manufacturers struggle to establish and maintain an effective CAPA process. An ineffective CAPA process leads to disastrous consequences like complaints, recalls, 483s, and warning letters. Additionally, an inefficient CAPA system leads to wasted time and resources.