Summary of a Corrective and Preventive Action (CAPA) Process l The Learning Reservoir

In this video, we delve into the fundamentals of CAPA, including its definition, purpose, and significance within the medical device industry.

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👉 If you want to learn more about the CAPA process, consider taking one of our CAPA courses. We offer flexible delivery methods.
CAPA courses delivered via ZOOM (LIVE Virtual Training):https://bit.ly/3VYFvoK
CAPA eLearning courses: https://bit.ly/3IM6UpK
In-Company CAPA courses: https://bit.ly/3CGmVtt

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🔔 𝗙𝗥𝗘𝗘 𝗲𝗕𝗼𝗼𝗸 "𝟳 𝗦𝘁𝗲𝗽𝘀 𝗥𝗲𝗾𝘂𝗶𝗿𝗲𝗱 𝘁𝗼 𝗳𝗶𝘅 𝗮 𝗕𝗿𝗼𝗸𝗲𝗻 𝗖𝗔𝗣𝗔 𝗦𝘆𝘀𝘁𝗲𝗺2🔔

𝗖𝗼𝗿𝗿𝗲𝗰𝘁𝗶𝘃𝗲 𝗮𝗻𝗱 𝗣𝗿𝗲𝘃𝗲𝗻𝘁𝗶𝘃𝗲 𝗔𝗰𝘁𝗶𝗼𝗻 (CAPA) is a critical part of a quality management system. Failure to comply with CAPA requirements can be costly for a company. CAPA system deficiencies routinely top the list of 𝗺𝗼𝘀𝘁-𝗰𝗶𝘁𝗲𝗱 𝗙𝗗𝗔 𝟰𝟴𝟯 𝗼𝗯𝘀𝗲𝗿𝘃𝗮𝘁𝗶𝗼𝗻𝘀 year after year.

If you are having problems with your CAPA system learn how to fix it by downloading our 𝗙𝗥𝗘𝗘 eBook now.

Get it here 👉 https://bit.ly/3I1ejAH

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