Mastering CAPA in Medical Device Manufacturing: Essential Steps

CAPA Webinar cover image

Webinar Title: Mastering CAPA in Medical Device Manufacturing: Essential Steps

Date: Tuesday, June 18, 2024

Time : 16.00 GMT / 11.00 EST

Description:

Join us for an insightful webinar where we will delve into the critical aspects of Corrective and Preventive Action (CAPA) in medical device manufacturing. This webinar is designed to equip professionals in the medical device industry with the essential knowledge and practical steps necessary to implement effective CAPA systems, ensuring compliance with regulatory requirements and enhancing overall quality management.

What You Will Learn:

  • Understand the key elements of CAPA and its significance for medical device manufacturers.
  • Learn about the essential steps needed to develop and implement an effective CAPA system.
  • Gain insights into identifying root causes and implementing preventive measures.
  • Explore strategies for continuous improvement through robust CAPA processes.

Who Should Attend:

  • Professionals involved in quality assurance, regulatory affairs, and compliance within the medical device industry.
  • Manufacturers, engineers, and executives responsible for product development and manufacturing processes.
  • Anyone seeking a comprehensive understanding of CAPA and its implications for medical device manufacturing.

Don’t miss this opportunity to enhance your knowledge and strategies for mastering CAPA in medical device manufacturing. Register now to secure your spot!

Meet our Speaker: Dr. Fiona Masterson, The Learning Reservoir 

Fiona Masterson headshot Dr. Fiona Masterson is a recognized subject matter expert in CAPA. With extensive experience in implementing CAPA programs, running CAPAs, and developing CAPA procedures, Fiona has successfully managed CAPA systems that ensure compliance and enhance quality management. She has been audited by the FDA on CAPA processes and consistently meets stringent regulatory standards. 

eLearning Course: Enhance Your CAPA Knowledge Further!

Dive deeper into Corrective and Preventive Actions with our eLearning course on 21 CFR 820.100 (Medical Device CAPA). This course is designed to provide an  understanding of CAPA requirements and best practices, equipping you with the tools needed to ensure compliance and improve quality management systems.

Why Enroll?

  • Gain expert insights and practical knowledge
  • Enhance your ability to manage and resolve quality issues
  • Improve compliance with FDA regulations

Don’t miss this opportunity to further your expertise and elevate your CAPA processes. Click the link above to enroll in the course today!

Can we help you?

At The Learning Reservoir, we’re dedicated to supporting professionals in the medical device industry with their training and educational needs. Whether you’re looking to enhance your team’s skills with customized training programs, need assistance with regulatory compliance, or have any questions about our services, we’re here to help.

Contact us today to learn more about how we can tailor our services to meet your specific needs and help you achieve your goals in the medical device sector.

Explore our YouTube Channel

Did you know we have a wealth of educational content available on our YouTube channel? Our channel is your go-to resource for valuable content on topics related to the medical device industry.

Subscribe to our channel today to stay up-to-date with the  best practices, and expert advice in medical device manufacturing and quality management. Don’t miss out on this opportunity to expand your knowledge and take your skills to the next level!

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