Medical device regulations – products as medical devices
Organiser: Bucks HSC Ventures
Venue: Online via zoom
Date & Time: 16 Jun 2020 - 10:30 am-12:00 pm
This event is for businesses and residents located in England due to eligibility rules on support.
This Bucks Health and Social Care Ventures programme workshop is fully funded and free to access . We have a number of workshops planned, if you would like to find out more then please check our website for further details of the support you can receive.
Are you developing a device for the health sector?
Are you unsure if you need to adhere to the Medical Device Regulations?
Or what the risk classification of your medical device is according to the Medical Device Regulations?
Then this workshop is for you.
The objective of this workshop is to learn the first key aspects of the medical device regulations: to determine when a product is a medical device and what the risk classification of the device is.
Who should attend?
People who are working in the area of medical devices/digital health solutions, including:
• academic researchers
• science students
• research council
• research services and tech transfer support
What will I learn?
By the end of the webinar delegates will be able to:
• Identify if a device / digital health solution is a medical device
• Classify a medical device according to the Medical Device Regulation (EU) risk levels
• Gain Hands on experience in using the regulatory tool: Oxford Global Guidance
Rita holds a PhD from the Medical Research Centre (MRC) at King’s College London. Throughout her career, Rita has been part of international multidisciplinary networks and has led large international initiatives in bridging the gaps between different scientific disciplines. Rita played a significant role in setting up and leading the training work stream within ELIXIR, European infrastructure for big data within biological research. She has also experience in working with big pharmaceutical companies. Rita previously worked for the University of Edinburgh and is currently overseeing the development of a data-driven tool to help navigate the medical device regulation at the Natural Interactions Lab based at the University of Oxford. She was involved in the REFORM research on ‘Data-driven healthcare: regulation & regulators’ and closely works with key stakeholders in the regulatory area, such as the MHRA and NHSx. She has given workshops on MDR classification for IEEE and EIT Health and has published on the topic of digital solutions for regulatory navigation.
Please note that the workshops are funded by European Regional Development Fund (ERDF) and are available to eligible SME applicants as part of the Bucks HSC Ventures programme. Sign up to these events to express your interest for an ERDF funded place and a member of our team will follow up with you. A maximum of one ERDF funded ticket per business is available. Please note that the event is for SMEs based in the UK and we will limit tickets to non-businesses or people outside of the UK.Book Now