ISO 13485 is an internationally recognised standard that sets out the requirements for a quality management system (QMS) for the design and manufacture of medical devices. Daniel Gardiner, quality manager, Alexander Battery Technologies, discusses.
Laura Friedl-Hirst, principal consultant and managing director, LFH Regulatory looks into accessing the UK market from a regulatory perspective and if it’s worth it.
Chris Whitehouse, political consultant and expert on medtech policy and regulation at Whitehouse Communications, advisor to medtech suppliers, chair of the Urology Trade Association, looks at the prognosis and treatment for the “broken” NHS.
After a historic general election in the UK, with the Conservatives ending up with the lowest number of seats in the party’s history, and Sir Keir Starmer becoming the nation’s Prime Minister, MTI reached out to contacts in the UK MedTech industry.
The 2024 Spring Budget announced a £4.2 billion boost for the healthcare sector. £3.4 billion of that is set aside for the NHS over three years to help the system work better, through increased investment in technology.
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, highlights a key UK government consultation that risked being buried by focus on the general election.
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, looks how the civil service general election shut-down impacts key medtech projects.
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, hails a review of the assessment system for digital health apps.
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications hails the issuing of the latest version of the new model for assessing value based procurement.
