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National Research Ethics Service
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Home
About us
About the National Research Ethics Service (NRES)
Who we are
How we work
How we are funded
Development of the research ethics service
About Research Ethics Committees (RECs)
The role of RECs
REC membership
How many RECs are there?
Different types of REC
Research applicants
Research ethics reviews by NHS RECs
Appointing authorities
Protecting participant safety
Building on Improvement
National Research Ethics Advisors Panel
Meet the panel
Panel papers
NREAP Minutes 2010
NREAP Minutes 2009
Accessibility
News and publications
News
Release of Adults lacking Capacity Toolkit
Publications
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NRES Training
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Applications
Approval requirements
Ethical review requirements
UK-wide system for ethical review
Requirements for ethical review under legislation
Requirements for ethical review under the policy of the UK Health Departments
Research tissue banks ('biobanks')
Research databases
Gene therapy and other advanced therapy medicinal products
Stem cell therapy
Social care research
Ministry of Defence research
NHS R&D approval
Other approvals
Access to Confidential Patient Information
Administration of radioactive substances
Clinical investigations of medical devices
Clinical trials of investigational medicinal products (CTIMPs)
Offender health research (including research in prisons)
Research involving human embryos and gametes
Storage of human tissue for research
International research
Research conducted outside the United Kingdom
Appointment of chief investigator
Sponsor’s legal representative
Integrated Research Application System (IRAS)
Site-Specific Assessment
Booking and Submitting your application
How to book
Where to book
Central Allocation System (CAS)
Local Allocation System (LAS)
REC Meeting Dates
NRES Committee Directory
Advanced search
After submission
Attending a REC meeting
After ethical review
Annual Progress Reports
Notification of Amendments
Examples of substantial and non-substantial amendments
Requirement for favourable ethical opinion
Notices of substantial amendment
Submitting notices of amendment
REC procedures for reviewing substantial amendments
Adding new sites and investigators
Urgent Safety Measures
Safety reports
Safety reports for CTIMPs
Safety reports for all other research
End of study and final report
Resubmission and Appeals
Providing feedback
Guidance
Clinical trials
Consent guidance and forms
Governance and directives
Guidance and good practice
Research guidance
Trials and procedure flowcharts
Frequently asked questions
Before applying
Applying for ethical review
After applying
Glossary
Proportionate Review
Patients and the public
Public involvement in RECs
Public involvement in research
Useful links
Contact us
NRES Office and Departmental Contact Details
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Raising concerns
