MPS provide international, medical device regulatory consulting and are able to act as your local representative in the UK, the EU and USA.
MPS can advise on gaining medical device clearances in the U.K., The EU and the USA. We can support you at all stages and have experience of working from the very earliest stages (eg University Spin-outs) all the way through Technical File Preparation Medical Device clearance and local territory representation.
MPS can work with your organisation to create full Technical File and Clinical Evaluation Filings for clearance of your device as a Medical Device in multiple territories.
MPS can act as your Responsible Person in the UK, EC-REP /AR in the EU and your local representative in the USA.
Our team consists of highly qualified and motivated professionals, who are all experts in their field. With many years of experience in the industry, they have the expertise to provide comprehensive, first-rate services to our clients.
With 25 years of working in the Medical Device, Healthcare Technology and Pharmaceutical industry, Ben is the engagement lead for the UK.
With 30 years of Medical Device experience, Gerhard heads up the EU engagements.
With 25 years of medical device experience, Reuben heads up US engagements.