12 September 2023

Managing Compliance and Requirements for Medical Device Solutions



Medical device product development has been a foundational element of the practice and betterment of medicine for about as long as mankind has been trying to heal people. Over the millennia, our medical devices have become more complex and powerful, and the same can be said for the regulatory environment.


Medical device risk management needs to be a living process that becomes a granular part of the entire product development process. Many of the challenges around risk management comes from using old technology – static written documents and spreadsheets – to track the complex and dynamic environment.


Traceability is the foundation of medical device risk management. A robust requirements management solution can support workflows and traceability through the design manufacturing and risk management relationships.


Register for this free breakfast seminar where we will address the challenges of complying with Medical Device Regulations and show how it's possible to maintain speed and quality in development projects in the Medical Device Industry.