Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, an advisor to MedTech suppliers, chair of the Urology Trade Association, and governor of the Anscombe Bioethics Centre, covers the launch of a new digital hub in the North of
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, an advisor to MedTech suppliers, chair of the Urology Trade Association, and governor of the Anscombe Bioethics Centre, highlights investment in new radiotherapy machines int
ReGelTec Inc., a company developing a percutaneous hydrogel implant for the treatment of chronic low back pain caused by degenerative disc disease, announced it has received CE Mark under the European Union Medical Device Regulation (MDR) for its Class III HYDRAFIL System for disc augmentation. This
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, an advisor to MedTech suppliers, chair of the Urology Trade Association, and governor of the Anscombe Bioethics Centre, highlights the priorities of NHS Supply Chain’s new Ad
Let’s be honest — if you’re in MedTech quality assurance or regulatory affairs (QARA), you’re probably drowning in paperwork right now. And it’s not your fault. The regulatory landscape has transformed dramatically, and traditional approaches just can’t keep pace anymore. We’ve seen an absolute tida
A new study published on Sunday 18th May has revealed tough financial decisions NHS leaders are making to balance their books and protect patient care. Researchers from The King’s Fund health and care charity spoke in detail to NHS leaders in England to understand the decisions being driven by tight
DNV, the independent assurance and risk management provider, has been recognised by the European Commission as a notified body for the certification of devices under the European Union’s In Vitro Diagnostic Regulation (IVDR). The designation increases capacity for certifying in vitro diagnostic devi
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, an advisor to MedTech suppliers, chair of the Urology Trade Association, and governor of the Anscombe Bioethics Centre, shares news of new robotic surgery systems approved by
Sarah Denham, Principal Consultant for Market Access and Patient Activation at IQVIA The NHS will be undergoing significant transformation following the announcement of the abolition of NHS England (NHSE), with responsibilities (including NHS Supply Chain) being moved into the Department of Health a
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, an advisor to MedTech suppliers, chair of the Urology Trade Association, and governor of the Anscombe Bioethics Centre, highlights must-attend opportunities for the MedTech s
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, an advisor to MedTech suppliers, chair of the Urology Trade Association, and governor of the Anscombe Bioethics Centre, looks at the key priorities for the new head of the UK
Dallas-based MedCAD has announced the 510(k) clearance of its AccuStride Foot and Ankle System, making these patient-specific precision devices available to surgeons. The unique design of these devices, coupled with the company’s proprietary software, will enable foot and ankle surgeons to correct m
