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Towards the end of January, WEISS staff attended and contributed to an excellent all-day workshop on medical devices. The aim of the workshop was to help staff explore the often-complex medical device regulatory pathways and to help understand and overcome the challenges of medical devices research and translation. WEISS’s Rachael Rodell ²¹²Ô»åÌýAdrien Desjardins (pictured) spoke at the workshop and discussed their own experiences of navigating regulatory pathways. This was a joint event organised by the IHE Research Infrastructure and Translation & Industry Delivery Groups, in collaboration with Õ¬ÄÐÊÓƵ Joint Research Office (JRO) and Translation Research Office (TRO).