Integrated MedTech Development from Requirements to Quality Documentation

Presented by

Szabolcs Ágai

About this talk

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. Agenda: 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

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Our regular webinars feature Intland's domain-expert partners, invited professionals from leading digital product development companies, and Intland's own experts. These live sessions (as well as their on-demand recordings) cover a variety of topics related to software-heavy product development in safety- or mission-critical industries. Join our webinars for cutting-edge insights & best practices from industry leaders. Find out how leading innovators are cutting product development time and costs, and how they use Application Lifecycle Management to gain a competitive edge.