Medical device regulations - product and risk

The objective of this workshop is to learn the first key aspects of the medical device regulations.

Are you developing a device for the health sector? Unsure if you need to adhere to the Medical Device Regulations? Or what the risk classification of your medical device is?

A free online course offered by the IKC and delivered by RegMetrics aims to demystify medical device regulations for up-and-coming innovators.

The purpose of this workshop is to discuss the first key aspects of the medical device regulations: how to determine when a product is a medical device and what the risk classification of the device is.

This course is free to attend for anyone working in the area of medical devices/in vitro diagnostic medical devices or digital health solutions, including: academic researchers, clinicians, science students, innovators, start-ups, SMEs, research councils, research services and tech transfer support.

About the trainer

Rita Hendricusdottir is the CEO of RegMetrics, a spin-out company from University of Oxford. RegMetrics develop digital solutions to support innovators navigate the regulations. One of the solutions is the RegMetrics platform, a digital tool to make it quicker and easier to understand how medical device regulations (both MDR and IVDR) apply to your product in order to obtain a CE mark certificate.

 

This event will be held online using Zoom. The event will take place on 23 March 10:00-11:30AM. For more details and to sign up, please follow the link below.