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National Research Ethics Service
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National Research Ethics Service - facilitating ethical research
Training and events
About the National Research Ethics Service
About us - About NRES
About us - Who we are
About us - How we work
About us - How we are funded
About us - Development of the research ethics service
About NRES - About Research Ethics Committees
About us - The role of Research Ethics Committees
About us - REC membership
About us - How many RECs are there?
About us - Different types of REC
About us - Research applicants
About us - Research ethics reviews by NHS RECs
About us - Appointing authorities
About us - Protecting participant safety
About us - Building on Improvement
National Research Ethics Advisors Panel
Meet the panel
Panel papers
NREAP Minutes 2011
NREAP Minutes 2010
NREAP Minutes 2009
NRES Publications
News and Publications - Publications
Publications - Announcements from NRES
Publications - NRES Bulletin and Compendium
Publications - RECs in the News
Quality Assurance and Quality Assurance Reports
Publications - Standard Operating Procedures
News and publications - Press Office contacts
Applications
Approval requirements
Applications - 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
Applications - NHS R&D approval
Applications - 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
Applications - International research
Research conducted outside the United Kingdom
Appointment of chief investigator
Sponsor’s legal representative
Applications - Integrated Research Application System (IRAS)
Site-Specific Assessment
Applications - Booking your application
Applications - How to book
Applications - Where to book
Applications - Central Allocation System (CAS)
Local Allocation Systems
NRES Committee Directory
NRES Committee Directory
Mergers, closures and REC name changes
REC Meeting Dates
Applications - After submission
Applications - Attending a REC meeting
Applications - 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
Applications - Safety reports
Applications - Safety reports for CTIMPs
Applications - Safety reports for all other research
Applications - End of study and final report
Resubmission and Appeals
After ethical review - Providing feedback
Applications - Guidance
Clinical trials directive and its implementation in the UK
Consent guidance and forms
Guidance - Governance and directives
Guidance and good practice
Research guidance
Phase 1 trials guidance
Applications - Frequently asked questions
Applications - FAQs: Before applying
Applications - FAQs: Applying for ethical review
Applications - FAQs: After applying / gaining ethical approval
Glossary
Proportionate Review Service (PRS)
HRA Ethics Officer Pilot
Contact us
NRES Office and Departmental Contact Details
NRES Committee Directory
NRES Committee Directory
Mergers, closures and REC name changes
Contact us - Raising concerns
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