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 Experts Talk webinar recording from 27 Nov 2019 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 webinar recording to learn more about using Intland’s tools (as well as the Medical Software Engineering Template and the Medical Audit & CAPA Template) to unify and streamline your medical device delivery lifecycle in a traceable manner.