ISO 13485: Best Practices and Challenges of Modernizing Document-based QMS

Join the webinar to learn more about

• Implementing an ISO 13485-compliant Quality Management System
• Challenges of implementing design control and traceability per ISO 13485
• Best practices of paperless QMS
• ISO 13485 compliance with codebeamer X

About our hosts

Laszlo Katona
Senior Solution Engineer at Intland Software
Laszlo is an ISO 13485 internal auditor and a certified Quality Management Specialist.

Danish Mairaj
Development Engineer at Resyca
Danish has over 10 years of medical device design and development experience with a strong background in MedTech regulatory compliance and quality management.

Abstract

For MedTech developers, ISO 13485 is a crucial standard that contains key requirements on Quality Management Systems for medical devices. Understanding this piece of regulation is vital to developing high-quality and safe medical technology products.

In this webinar (Part 2 of our 2-episode series on ISO 13485), QMS experts from Resyca and Intland Sofware will focus on the practical aspects of going paperless with ISO 13485-compliance. Join us to gain best practices for modernizing document-based workflows in MedTech QMS. The webinar will provide a demonstration of how Intland’s codebeamer X platform can help manage QMS-related processes in a digital environment.