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.

Their 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.

MTIF regularly collaborates with IMed Consultancy to attend and deliver workshops and conferences. IMed Consultancy play an important role in ensuring MTIF can offer our clients a fully rounded and comprehensive service.