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    Aug 25, 2021

    JOIN WITH US FOR LIVE WEBINAR - "Corrective and Preventive Action (CAPA)"

    in Webinars

    Live Webinar: Corrective and Preventive Action (CAPA) When: Wednesday September 22, 2021 - 01:00 PM Duration: 60 Minutes.

    Register Now


    Corrective and Preventive Action (CAPA) is a requirement under international standards such as ISO 13485:2016, ISO 9001:2015 and FDA under 21CFR 820 & is typically found in FDA Warning Letters. This webinar will define and explain Corrective Action and Preventive Action requirements as found in ISO 13485 and FDA requirements. It will include discussions on root cause analysis, quality system trending, corrective action effectiveness, and how CAPA is critical to be linked to other parts of the quality system including customer complaints, manufacturing nonconformities, customer feedback, supplier performance, etc. Lastly, this course will include the consequences of poor adherence to these pro


    Areas Covered in the Session:

    Regulatory Requirements

    Correction vs. Correction Action

    CAPA & Risk Management

    Determining Root Cause

    Tools for Root Cause Analysis

    Corrective Action Effectiveness

    Quality System Trending

    Linking CAPA to other parts of the QMS (Quality Management System)


    Register soon because space is limited.

    We hope you’re able to join us!

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