FDANews Webinar: Perform Effective Investigations and CAPAs Key Steps to Avoid Regulatory Citations
June 18, 2019
The Corrective and Preventive Action (CAPA) process is the heart of any quality management system. And yet, year after year, CAPA violations are the most frequently observed Quality System subsystem cited by FDA regardless of the manufacturers shape or size.
Susan Schniepp, RCA Distinguished Fellow, will discuss the importance of effective CAPA and investigations management and share best practices for creating effective programs.
Use Promo Code “VIP20” for 20% off registration.