Mastering ISO 13485:2016: Basics of Quality Management Systems for Medical Devices

Mastering ISO 13485:2016: Basics of Quality Management Systems for Medical Devices

Webinar Title: Mastering ISO 13485:2016: Basics of Quality Management Systems for Medical Devices

Date: Tuesday, Sept 10, 2024

Time : 16.00 GMT / 11.00 EST


Join us for an insightful webinar where we will delve into the critical aspects of ISO 13485:2016, the international standard for quality management systems specific to the medical device industry. This webinar is designed to equip professionals in the medical device industry with the essential knowledge and practical steps necessary to understand and implement ISO 13485:2016.

What You Will Learn:

  • Understand the key elements of ISO 13485:2016 and its significance for medical device manufacturers.
  • Learn about the essential steps needed to develop and implement a quality management system compliant with ISO 13485:2016.
  • Gain insights into maintaining and continuously improving your quality management system.
  • Explore strategies for achieving and maintaining certification to ISO 13485:2016.

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 ISO 13485:2016 and its implications for medical device manufacturing.
  • Don’t miss this opportunity to enhance your knowledge and strategies for understanding and implementing ISO 13485:2016. Register now to secure your spot!

Note: By registering for this webinar, you agree that your supplied contact information can be shared with the event presenter for the purpose of contacting you regarding this webinar and related information/products discussed within. The event host, Learning Reservoir, may also contact you regarding future webinars, events, newsletters, and related marketing materials. Please review our Privacy Policy for more information.

Meet our Speaker: Dr. Fiona Masterson

Fiona Masterson headshotDr. Fiona Masterson brings extensive expertise in quality management systems within the medical device industry. With a robust background in companies adhering to ISO 13485:2016 standards, Fiona has served as a lead auditor for ISO 13485, ensuring compliance and driving continuous improvement in quality processes. Her practical insights and experience in implementing ISO 13485:2016 make her a valuable resource for understanding and optimizing quality management systems for medical devices.

eLearning Course: Expand Your ISO 13485:2016 Expertise!

Take your understanding of ISO 13485:2016 to the next level with our comprehensive eLearning course, “Introduction to ISO 13485:2016 Online Training Course.” This course is designed to provide you with a thorough foundation in the essential aspects of ISO 13485:2016 standards, equipping you with the knowledge and skills needed to excel in quality management for medical devices.

Why Enroll?

  • Gain a solid understanding of ISO 13485:2016 standards
  • Enhance your ability to develop and manage effective quality management systems
  • Improve compliance and quality assurance within your organization

Don’t miss this opportunity to advance your knowledge and skills in ISO 13485:2016. 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.

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