UOVO medtech is led by Peter Brady, a medical device/IVD regulatory consultant with a deep understanding of technology, regulation and the medical devices industry. Peter has a first degree in Engineering, a Master’s in Computer Science and Mathematics and has successfully completed a programme in business studies at Copenhagen Business School and has a postgraduate diploma in Digital Transformation from MIT.
He has held senior positions in healthcare technology with Philips Healthcare, Getinge and Elekta Oncology Systems and has held CTO positions in a number of medtech start-ups. He has also held managing consultant positions with world-leading technology consultancies in Cambridge, UK. Peter is also a freelance subject matter expert in medical device software and risk management with a leading EU/UK Notified Body. He has won two IET Technology Innovation awards for novel digital health technologies.
His experience includes regulatory and technology strategy, product development roadmaps, management systems for medical device development and information security in healthcare applications, technical file development, software development processes, usability engineering processes and risk management. He is a specialist in safety critical systems and software development and using agile methods to develop safe, reliable and robust software. His experience covers radiotherapy, proton therapy, medical imaging, digital health technologies, Software as a Medical Device (SaMD), AI/ML technologies, implantable devices, in-vitro diagnostic technologies, surgical robotics, therapeutic devices and intraoperative molecular imaging.