TudorRose Consulting

  • Clinical Research Organisation

Our company provides commercialisation services, including regulatory and clinical trial consulting and co-ordination, for medical devices and prescription medicines.

Global:

  • Strategic commercialisation plans
  • Site selection
  • HREC applications
  • Site initiation and training
  • Monitoring and closeout
  • Clinical Data Management
  • Statistics
  • Medical Writing
  • Regulatory agency meetings
  • Regulatory submissions
  • 3PL and manufacturer audits
  • Quality system design and implementation
  • Pricing and reimbursement
  • Capital raising

Clinical trials should be viewed as part of a comprehensive commercialisation strategy and we are able to assist in the design of your overall development program, providing targeted expertise, as needed, at every step.

The mission of TudorRose Consulting is: Ethical and timely commercialisation of therapeutic products to enhance patient outcomes.