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Discover Best Practices for Medical Device Success

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Join Our Free Webinar Series: The Building Blocks of Success

Empowering Excellence in the Medical Device Industry

Welcome to “The Building Blocks of Success” webinar series! Designed to empower excellence in the medical device industry, each session provides valuable insights and practical guidance on essential topics. 

Whether you’re new to the industry or a seasoned professional, join us to explore foundational elements crucial for driving innovation, compliance, and continuous improvement within medical device companies. Don’t miss this opportunity to learn from industry experts. Register now and unlock your full potential in the medical device industry!

CAPA Webinar cover image

Mastering CAPA in Medical Device Manufacturing: Essential Steps

Date:  Tuesday, June 18, 2024

Time : 16.00 GMT / 11.00 EST

Don’t miss this opportunity to gain expertise in mastering CAPA and optimizing quality management processes in medical device manufacturing. Register now to secure your spot!D

Mastering Internal Audits

Mastering Internal Audits - Best Practices for Medical Devices Companies

Date: Tuesday, June 25, 2024

Time : 16.00 GMT / 11.00 EST

In this webinar, we’ll delve into the fundamental principles and requirements of ISO 13485:2016, providing you with a comprehensive understanding of how to establish and maintain an effective quality management system for medical devices. 

21 CFR 820 Compliance - Essential Steps for Medical device manufacturers

21 CFR Part 820: Essential Steps for Medical Device Manufacturers

Date:  Tuesday, July 02, 2024

Time : 16.00 GMT / 11.00 EST

Don’t miss this opportunity to gain expertise in mastering CAPA and optimizing quality management processes in medical device manufacturing. Register now to secure your spot!D

ISO 13485 Webinar image

ISO 13485:2016 - Understanding the Basics of Quality Management Systems for Medical Devices

Date: Tuesday, July 09, 2024

Time : 16.00 GMT / 11.00 EST

In this webinar, we’ll delve into the fundamental principles and requirements of ISO 13485:2016, providing you with a comprehensive understanding of how to establish and maintain an effective quality management system for medical devices.