Working With Us
What Can We Do For You?
We are supported by the University of East Anglia, Norfolk and Norwich University Hospital Trust and the NIHR. Our remit is to support local and national investigators to deliver high quality trials that answer important clinical questions. Further information about the NCTU is available in our
Trial activities we will typically be involved in are described below. We can only act as your official Clinical Trials Unit if we have oversight of the main trial activities. Please note that if you only require randomisation and database support, this may be available, depending on capacity at the discretion of the CTU Director. Provision of data services alone does not enable a trial to be an official Norwich CTU trial.
Trial activities we are involved with
For complex single site and multi-centre randomised controlled trials (RCTs)
Preparation and submission of grants for CTU trials
This includes study and participating site set-up, preparation of all essential study documents, regulatory and ethics submissions, preparation of annual reports etc.
Including data management, data quality assurance, preparation of CRFs and database programming (set up and maintenance).
Including development of monitoring plans and remote monitoring
Including sourcing and re-ordering
Trial Steering Committees, Data Monitoring Committees, Trial Management Groups, Investigator meetings, End-point review meetings
MHRA inspections, CTIMP studies and regulatory submissions