Mastering CAPA

The Mastering CAPA (Corrective and Preventive Actions) Workshop is a 4-day intensive theory and hands-on workshop providing a foundation for medical device students and industry professionals to understand global medical device regulations & technical, compliance and regulatory elements.

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Become MedTech Industry Ready in Weeks

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Mastering CAPA in Medical Devices with a Risk Based Approach
It's time to start prioritizing risks | A 4-day virtual intensive workshop

Date: June 11th - June 14th, 2024

Time: 1pm - 5pm EST

Location: Virtual

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Become MedTech Industry Ready in Weeks

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Mastering CAPA in Medical Devices with a Risk Based Approach

This unique CAPA Workshop will help participants gain practical tools on how to avoid warning letters, measure the health of your medical device business as well as to ensure consistent medical device business processes and external quality audit readiness. Using real-world examples, participants gain rapid knowledge and key takeaways by walking through the global regulations related to the CAPA process and the new #MakeCAPA Cool framework introduced by the MDIC (Medical Device Innovation Consortium) in May 2023

The Goal

The primary goal of the CAPA Workshop is to boost your career in medical device quality, operations, regulatory or R&D. Participants will quickly gain strong understanding of global medical device requirements along with proper corrective and preventive actions.

4 days only!

This super-efficient 4 half-days CAPA Bootcamp prepares students and industry professional to understand CAPA global medical device guidelines and quality system regulations

Our Partner

This Bootcamp is hosted by Enerxen, a pivotal leader in Life Sciences Consulting. Enerxen's quality, regulatory, and product development consulting services support companies in bringing compliant, high-quality products to market through expert guidance and efficient processes.

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CAPA in Industry

The Corrective and Preventive Action (CAPA) process in medical devices is a systematic approach to investigating, addressing, and preventing the recurrence of issues. It involves identifying the causes of non-conformities or deviations, implementing corrective actions to prevent reoccurrence, and preventive actions to deter future occurrences, ensuring compliance with industry regulations and maintaining high standards of product safety and efficacy. CAPA is essential for continuous improvement in the quality management systems of medical device manufacturing. By mastering the CAPA process, MedTech companies can enhance their overall quality management syste,, mitigate risks, and continuously improve their prodcuts and processes. Ultimately safeguarding patient wel-being and maintaining industry credibility