IMed Consultancy Ltd.

IMed Consultancy is a highly knowledgeable medical devices regulatory consultancy with key experience in Regulatory Affairs and QA in medical devices, including Class III, active & implantables, Software as a medical Device (SaMD) and IVDs, founded in 2012. Our team of highly skilled and experienced medical device regulatory professionals, whose focus on client relationships and industry expertise, combine to offer an outstanding yet flexible global regulatory service and consistently support all types of businesses in meeting the requirements of different international regulatory environments from the UK to the EU and the USA, but also further afield.