AbNovo Ltd is a regulatory consultancy focusing on requirements for medical devices in the European Union and the United Kingdom
Our one stop shop approach, using network partners, enables us to resolve problems arising throughout product and business life cycles.
Abnovo can also act as a UK Responsible Person for non-British manufacturers as well as a legal representative for clinical trials taking place in the United Kingdom.
Abnovo is a member of:
The European Association of Authorised Representatives (EAAR)
The UK Responsible Person Association (UKRPA)