Following last year's panel session on the latest regulatory updates from the world of medical technology, another live episode follows up on the latest developments and timings of regulations that you need to know ahead of developing your innovation. 

Topics that will be covered include: 
- The latest developments surrounding UK requirements
- How recent fast-track approvals from EU, U.S. and Japan may affect the UK
- International regulations: The effect on UK innovators, and the effect on overseas innovators coming to the UK
- The similarities and differences with medical device and pharmaceutical sectors
- Software as a medical device (Samd) challenges
- Q&A