The UK’s Medicines & Healthcare products Regulatory Agency will continue to recognize CE Marked products for use in the country for a limited time following a ‘no deal’ Brexit scenario, according to new guidance from the agency.
Safety and quality are non-negotiable in the medical devices industry. More and more, organizations are being put under a microscope, expected to demonstrate their quality management processes and ensure best practices in everything they do. At genae, we tap into our wide range of quality and regulatory experience and expertise to guide you through every stage of your clinical project. Download this case study and discover our quality expertise.