Integrated MedTech Development from Requirements to Quality Documentation

Unifying the numerous complex stages of product development is a vital challenge for innovators of medical technology. An integrated approach to MedTech product delivery is the key to navigating traceability, risk management, and quality control in a way that supports regulatory compliance and high product quality.

Watch this on-demand Experts Talk webinar with Szabolcs Agai, Intland’s Functional Safety Expert and Quality Consultant. Learn more about the best practices of implementing a fully integrated delivery process from product specification through engineering, software design, and quality documentation all the way to successful compliance audits.

Watch this practical-minded on-demand webinar to learn more about using Intland’s tools and Medical Software Engineering Template to unify and streamline your medical device delivery lifecycle in a traceable manner.

In this on-demand webinar, we cover the topics of:

• Adopting an integrated and traceability-focused approach to medtech product development
• Tracing requirements and other artifacts through each stage of product delivery
• Best practices of tying in quality engineering with product development every step of the way
• Navigating quality management as per ISO 13485 and relevant standards