Introduction

The ability to set up studies rapidly is central to making the NHS an internationally competitive environment in which clinical research can take place. A system is being developed which will ensure clinical research studies are approved quickly through a consistent and streamlined process whilst addressing all quality assurance and statutory research requirements.

It will:

• Reduce the duplication in the NHS review process
• Provide a single point to which sponsors and investigators need to apply for NHS permission to start multi-site and single site studies
• Ensure clarity regarding the roles and responsibilities of sponsors, investigators, Networks and Trusts.

The National Institute for Health Research (NIHR) Coordinated System for Gaining NHS Permission (NIHR CSP) will be rolled out during 2008. It will be delivered by a national CSP Unit based in the UK Clinical Research Network Coordinating Centre. The Unit will be supported by teams of staff based within the 25 Comprehensive Local Research Networks who will work closely with their constituent NHS organisations.