Are you interested in medical device regulation? Want to know more about the NHS adoption pathway, market assessment or PPIE?
We are running three courses online as part of our winter 2021 programme of learning.
These sessions will give you an introduction to different aspects of medtech innovation, helping to navigate the pathway of NHS adoption, learn more about medical device regulation, and the importance of patient and public involvement and engagement (PPIE) in research.
NHS strategy and adoption/market assessment
22 and 23 November 9:30am – 12:30pm
This course will look at how to start innovating in the NHS context, and will provide you with the practical tools to assess your research for potential in a healthcare setting.
Using real case studies, we’ll explore how innovation works in the NHS, the opportunities and potential pitfalls to avoid when developing your research into something that can benefit patients.
Regulatory affairs for medical devices
29 and 30 November 9:30am – 12:30pm
This course is an introduction to medical devices and the regulatory requirements for placing medical devices on the market and CE marking of devices.
It will help you to understand the regulatory path to CE marking a device, deciphering all the regulatory jargon and understanding the new Medical Device Regulations in Europe as well as the UK legislation.
Patient and public involvement and engagement
9 December 9:30am – 12:30pm
This course aims to increase knowledge about how to involve patients, the public and carers in the development and delivery of medtech research.
The session will use hands on activities and examine real life case studies of effective PPIE methods.