Event Resources Add Event
Loading Events

« All Events

Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data

May 22 @ 1:00 pm - 2:00 pm

| $199

Overview
Year after year, CAPA is the subsystem cited most frequently during FDA inspections. A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer. A system that identifies and eliminates nonconformances and potential nonconformances enables both regulatory compliance and cost savings.
Why Should You Attend
This webinar will identify the most common elements identified as deficient by FDA, and provide recommendations for how to provide clear, concise documentation to assure FDA your firm has addressed these in your quality system. This webinar also provides recommended forms to assure that in addition to being able to illustrate compliance; your firm’s CAPA system is useful and meaningful.
Areas Covered in this Webinar
Regulatory Requirements
FDA QSR
ISO 13485
Elements of a cross-procedural CAPA program
Applications of CAPA
CAPA Data and best practices for its use
Application of risk management to CAPA program

For more detail please click on this below link:

http://bit.ly/2p03szK

Email: referrals@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Fax: +1-516-900-5510

Details

Date:
May 22
Time:
1:00 pm - 2:00 pm
Cost:
$199
Website:
http://bit.ly/2p03szK

Venue

2754 80th Avenue, New Hyde Park, NY 11040
2754 80th Avenue, New Hyde Park, NY 11040, New York, NY 11040 United States
Phone:
5169005509
Website:
http://bit.ly/2oFO1bx

Organizer

Compliance Global Inc.
Phone:
5169005509
Email:
Website:
http://bit.ly/2oFO1bx