Arrow In this section

"The NHS aspires to the highest standards of excellence and professionalism…through its commitment to innovation and to the promotion, conduct and use of research to improve the current and future health and care of the population." – NHS Constitution

Initiation – Setting up research studies and recruiting the first patient

All clinical trial research that takes place in the NHS has to have approval from an NHS Research Ethics Committee, the MHRA if it is a drug or device trial, and the host organisation via its NHS permission.  NHS permission from MFT ensures everything is in place for the research to go ahead from a regulatory and practical perspective. We work hard at streamlining our research processes to set up clinical trials quicker, whilst maintaining robust governance procedures according to the Research Governance Framework. You can see how we perform against the NIHR benchmark of 70 days from a valid application to first patient recruited: research initiation. This benchmark has been prescribed by the NIHR and, in order to pinpoint areas for improvement from a local and national level, reasons are assigned that cause delays.

Most recent performance in initiating and delivering clinical research data.

To “time and target” delivery data

Working with Industry our Trust agrees to try and find a certain number of participants in a particular timeframe for their trials.
The NIHR are encouraging transparency and below is our data for delivering “to time and target”.