Webinar: 3 Hour Virtual Seminar- Best Practices for Deviation Training When: Wednesday Apr 21, 2021 - 11:00 AM EDT Duration: 3 Hours.
Deviation investigations and CAPAs are a very common topic to be reviewed during FDA investigations. Ensuring the firm has robust and complete write-ups of these situations is key to a successful audit. Having inadequate investigations or ineffective CAPAs could potentially cause some severe issues for the company and may sometimes result in warning letters, consent decrees or recalls.
Objectives Of the Session:
Outline the requirements of the Deviation and procedure including the deviation report
Choose the most appropriate Root Cause Analysis methods for the situation
Discuss how to conduct the deviation and the tools to be used in the process
Why Should you Attend:
This webinar will help attendees understand the fundamental steps of a deviation investigation with focus on using facts and objective evidence to arrive at root cause and CAPA. This webinar will focus on how to avoid the pitfalls that may occur during FDA inspections and help eliminate 483 observations. Learn how to identify and avoid potential pitfalls during deviation investigations.
Contact Person: SAM
+1 3156320735