- TypeWebinar
- Location New York, United States
- Date 22-05-2017
Manufacturing
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
For more detail please click on this below link: http://bit.ly/2p03szK
Email: [email protected]
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Fax: +1-516-900-5510
During this live CAPA compliance training, the speaker will discuss the importance, requirements, and elements of a CAPA program. Book now!
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