Medical Devices 2011 - Corrective and Preventive Actions(CAPA) - 8 Steps to Achieve Compliance

In this CAPA training webinar, we will focus on ideas that will help identify effective methods designed to improve your response to process deviations and help you develop a standardized plan to fully resolve discrepancies so they do not recur.

Since regulatory inspectors look very closely at non-conformances you have to have a robust CAPA process and its success is dependent on two things: a well-thought out strategy, and employees specifically trained to handle the discrepancies.

This CAPA webinar will teach specific techniques to ensure organizations are prepared to fully investigate and prevent out-of-specification situations. We will focus on standardizing your investigatory techniques so that every deviation is handled the same way. Further, you will learn techniques that will help you create solid CAPAs that are unambiguous and complete. We will also examine applicable warning letters and 483s so that your company doesn’t make the same mistakes as other organizations. By building compliance into every aspect of your operation, you can concentrate on getting more quality product out the door.