For the past few years, the UK regulatory landscape has been uncertain. UKCA was coming. CE was going. Timelines kept shifting. Now there is clarity. The Medicines and Healthcare products Regulatory Agency has confirmed that CE-marked medical devices will continue to be accepted in Great Britain for an extended period. On the surface, this looks

In MedTech, failure rarely comes from bad science. It comes from misalignment between innovation, regulation, and real-world use. Developing a medical device is one of the most complex product journeys in any industry. Small early decisions compound quickly. What looks like a minor shortcut in month three can become a multi-million-pound delay by