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Innovation Breakfast: What happens when you get the right people in the room
Kicking off at 9am sharp, last Thursday, we hosted our first Innovation Breakfast of the series at The Forge in Bristol. What began as a short presentation quickly turned into something much more valuable: a genuine cross-industry roundtable where leaders compared challenges, shared insights and explored the real tensions shaping innovation today.
The session followed Chatham House Rules but we can say this: the room brought together an unusually diverse mix of perspectives. From scientific research and semiconductor innovation to advanced engineering, defence, media, public sector policy and cutting-edge tech businesses, we had leaders at the table who rarely get
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Navigating MedTech regulations when undertaking a medical software development project
When medical devices and software products are created, all parties involved must have a firm understanding of compliance regulations, conformity marking and classification types, to ensure that the development process aligns with the highest standards of safety, efficacy, and quality.
Unfortunately, recent and proposed changes to these regulations following the UK’s exit from the EU, make it increasingly difficult to source the most relevant and reliable information. Some documents have undergone changes and adaptations, while others refer to existing literature.
To help guide you through the process, we’re sharing some of the most up-to-date resources so that you know how
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