Join us for the grand final series episode, “Commercialization & Implementation; Part-2 Preparing for Launch”. In this final episode, we welcome Andrew Martin, Vice President of MIDI, to delve into the critical aspects of RISK MANAGEMENT (ISO 14971) and its integration within our development framework.
What You’ll Learn:
- Comprehensive Overview: Recap the series by revisiting key topics such as class identification, planning, requirements, and design control methods. Understand how each element ties into the overall INNOVATION ROADMAP™.
- Focus on Risk Management: Discover how MATRIX-ALM, our advanced tool, is utilized to document and manage risk. Andrew Martin will guide you through risk analysis, production, and post-production activities, emphasizing the importance of effective risk management in medical device development.
- Practical Insights: Learn how to apply ISO 14971 standards to identify, evaluate, and mitigate risks throughout the product lifecycle, ensuring compliance and enhancing device safety.
Why Tune In?
This episode is crucial for developers, engineers, and industry professionals looking to master risk management in the context of medical device development. Gain practical knowledge on leveraging MATRIX for comprehensive risk documentation and management, completing your understanding of the INNOVATION ROADMAP.
Be at the Forefront of Medical Device Innovation.
Don’t miss this concluding episode as we wrap up our exploration of the INNOVATION ROADMAP. Equip yourself with the insights needed to manage risk effectively and ensure your medical device development process is both innovative and compliant.
Listen Now to complete your journey with the INNOVATION ROADMAP and stay at the forefront of medical device development.