NHS Imperial College and Imperial College Healthcare NHS Trust sponsorship process
All healthcare research projects must gain sponsorship approval from the Research Governance and Integrity team (RGI team) on behalf of Impeial College or Imperial College Healthcare NHS Trust.
Research projects must apply for sponsorship with Imperial College or ICHT whether they are a clinical trial of an IMP or device, human tissue project, observational or epidemiological study.
The RGIT aim to give you a response on registration within 5 working days where possible subject to pressing deadlines of which we are made aware.
IC sponsorship
Registration is required as it allows the RGIT to:
- Assess for Imperial College or Trust sponsorship of your project (as applicable)
- Confirm or arrange appropriate insurance cover for your study
- Discuss research governance issues with you if required
- Ensure you have the necessary regulatory approvals
- Have an overview of the RGIT’s clinical research portfolio and respond to monitoring/audit requests by regulatory authorities
Registration needs to occur prior to submission of your ethics application and before project initiation
NHS Imperial College and Imperial College Healthcare NHS Trust sponsorship process
All healthcare research projects must gain sponsorship approval from the Research Governance and Integrity Team (RGIT) on behalf of Imperial College or Imperial College Healthcare NHS Trust.
Research projects must apply for sponsorship with Imperial College or ICHT whether they are a clinical trial of an IMP or device, human tissue project, observational or epidemiological study.
The RGIT aim to give you a response on registration within 5 working days where possible subject to pressing deadlines of which we are made aware.
NHS Imperial College and Imperial College Healthcare NHS Trust sponsorship process
Registering is a simple process for projects in which you require the College or Trust to act as sponsor.
Please complete the following documents and send them to RGIT inbox:
- A copy of the RGIT_SOP_012_Protocol_design_v12.pdf
- A copy of the IRAS form
- And the participant information sheet and consent if applicable: RGIT SOPs
- All study other related documentation i.e. questionnaires
- An Organisational Information Document and Schedule of Events (or SoECAT if NIHR adopted) for sites outside of ICHT