In this insightful episode, “Commercialization & Implementation; Part-1 Preparing for Launch,” we continue the exploration of the INNOVATION ROADMAP™ for medical device development. In the previous episodes we have journeyed through the initial stages of market exploration and technological innovation. This has allowed us to investigate opportunities and develop exploratory technology prototypes without the constraints of FDA-QSR and ISO-13485 regulatory controls.
Key Episode Highlights:
- Introducing Wolfgang Huber: This episode features Wolfgang Huber, Co-Founder of Matrix Requirements, who shares insights into their innovative cloud-based tool designed to support companies through complex development processes.
- INNOVATION ROADMAP: Discover how to transition from exploratory stages to structured development, where Design Controls and Risk Management come into play. Learn how to seamlessly integrate regulatory requirements into your development workflow, leveraging insights from earlier explorations.
- Practical Application: Explore how Matrix Requirements’ tool can streamline your process, ensuring compliance while maintaining the agility to innovate. Wolfgang discusses how this tool enhances efficiency, simplifies documentation, and supports alignment with FDA-QSR and ISO-13485 standards.
Why Listen?
This episode is a must for medical device developers and innovators looking to bridge the gap between exploratory development and formal regulatory compliance. Gain practical knowledge on how to advance your development process while integrating essential regulatory controls effectively.
Stay on the Path of Innovation.
Tune in to advance your understanding of the INNOVATION ROADMAP and discover tools and strategies to navigate the critical transition to regulated development stages. Learn from industry experts and enhance your approach to medical device innovation.
Listen Now and continue your journey towards successful and compliant medical device development.