Experts Talk: Integrated MedTech Delivery from Requirements through Design to Quality Documentation

What you can learn:

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.

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

Attend this practical-minded 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.

The webinar’s agenda:

In this Experts Talk session, we’ll 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

Our webinar is intended for:

Project Managers and Team Leaders, Product Quality and Test Engineers, Heads of Testing & QA teams, Embedded Software Developers, Business Analysts, Regulatory Compliance Analysts