Join us for a hybrid in-person and on-demand session designed to provide international HealthTech companies with an expert overview of the key milestones for both UK and US regulatory systems.
The session will feature a prestigious panel, including Graeme Tunbridge, Director of Devices at the MHRA, to provide their unique insight into the synergies and opportunities presented by the respective regimes, which have been emphasised by the UK’s post-Brexit trade ambitions.
The event will be made up of an introduction to the key milestones in the UK & US Regulatory Systems, before a fireside chat panel discussion with:
We will then look to respond to any pre-submitted questions, before an open Q&A and networking session. Please click here to submit a question.
The event will be recorded so if you are unable to make it please register to receive a copy of the recording.
If you have any questions please use the following details: