Westminister Technologies UK is an independent institution of BioMedical Engineering Consultancy firm
WTUK is based in the UK and has an association in the Middle East. Our active, highly-Qualified engineers are capable of handling regulatory affairs issues and can guide and help the manufacturers for registration of the medical device into Great Britain.
Our Process
We Provide best services
Our expert team of biomedical engineers and regulatory affairs will make sure all the documentation and other stuff is right in place in order to avoid any delays.
REGISTRATION
REVIEW/APPLY
APPROVAL/REJECTION
CERTIFICATION
EU-based Authorized Representatives
EU-based Authorized Representatives are no longer recognized in the Great Britain. Great Britain-based Authorized Representatives are no longer recognized in the EU. This means that they are not able to carry out tasks on the manufacturer’s behalf for the purposes of placing devices on the EU market and/or Great Britain Market. If you are a manufacturer based outside the EU and you currently have only a EU-based Authorized Representative, you must appoint an Authorized Representative based in the Great-Britain.
We can provide you the professional services in order to register your device in MHRA on a fast track bases. Our expert team of biomedical engineers and regulatory affairs will make sure all the documentation and other stuff is right in place in order to avoid any delays.
