Session: The Key to Successful IoMT: Quality and Compliance at Every Step
True chipping and cyberpunk are closer than you might imagine. Imagine being able to watch movies without a screen or listen to music directly in your head, without headphones. Controlling your smart home with just your thoughts, just like Neo from The Matrix learned to fly a helicopter in seconds. With neural brain interfaces, this is becoming a reality. The potential to restore sight to the blind, hearing to the deaf, movement to the paralyzed, and speech to the mute is within reach.
Therefore, the importance of designing safe and usable medical devices cannot be overstated. Such devices have the potential to greatly improve healthcare outcomes and increase access to care, but only if they are designed with the user in mind and meet the necessary safety and performance standards.
- to learn about the exciting and rapidly evolving field of medical devices, with a particular focus on the impact of IoMT
- to gain an understanding of the complex regulatory landscape for IoMT
- to understand the key considerations for ensuring product quality and safety
- to have the chance to dive into real-world scenarios and consider different perspectives on the issues facing the industry
Marina Daineko is a Medical Device Quality and Compliance Expert at EPAM Systems. In this role she is responsible for the quality and compliance aspects for medical devices for purposes of product registration and safety assurance. Marina holds a MSc in Analytical Chemistry.
With over eight years of medical device experience, a knack for understanding chemistry and an insatiable appetite for helping others use safe products, Marina knows how to navigate the complex regulatory landscape for medical devices.