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Action to enhance visibility of clinical research delivery against the UK government’s commitment to reduce the set-up time for clinical trials to less than 150 days
UKCRD Priority to streamline and reform the set-up and delivery of clinical trials Frequently Asked Questions (FAQs)
Guidance on detailed definitions and processes for site-level performance reporting
National Contract Value Review (NCVR) process improvement
NCVR update for sponsors and CROs
NCVR Update for NHS Organisations (and HSC in Northern Ireland)
Consolidated UK-wide guidance page for study set-up
Q and A from the National Contract Value Review (NCVR): Process Update Webinar
NCVR Transition Principles
Study Set-Up: Trust level set up report
Study set up: Trust level data archive
Study Set-Up: Policy Statement
UK Guidance for Study Set-Up
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Study Set-up
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UKCRD Priority to streamline and reform the set-up and delivery of clinical trials Frequently Asked Questions (FAQs)
NCVR Transition Principles
Q and A from the National Contract Value Review (NCVR): Process Update Webinar
Consolidated UK-wide guidance page for study set-up
National Contract Value Review (NCVR) process improvement
Joint UK guidance on interpretation of IR(ME)R in NHS research
Updates to RDN Portfolio Eligibility Criteria
NIHR support for 150-day study set-up for clinical trials
Guidance on detailed definitions and processes for site-level performance reporting
Bulletin: Action to enhance visibility of current research delivery set up activities in the UK
Action to enhance visibility of clinical research delivery against the UK government’s commitment to reduce the set-up time for clinical trials to less than 150 days
Webinar: Study Set-Up Plan update Progress and next steps
Study Set-Up Plan: Questions
Study Set-Up Plan: Phase 2 Completed
Bulletin: Requirement for use of the Schedule of Events Cost Attribution Tool (SoECAT) and the unmodifiable existing model Non-Commercial Agreement (mNCA) and Organisation Information Document (OID)
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Action to enhance visibility of clinical research delivery against the UK government’s commitment to reduce the set-up time for clinical trials to less than 150 days
UKCRD Priority to streamline and reform the set-up and delivery of clinical trials Frequently Asked Questions (FAQs)
Guidance on detailed definitions and processes for site-level performance reporting
National Contract Value Review (NCVR) process improvement
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NCVR update for sponsors and CROs
NCVR Update for NHS Organisations (and HSC in Northern Ireland)
Consolidated UK-wide guidance page for study set-up
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NCVR Transition Principles
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UKCRD Priority to streamline and reform the set-up and delivery of clinical trials Frequently Asked Questions (FAQs)
NCVR Transition Principles
Q and A from the National Contract Value Review (NCVR): Process Update Webinar
Consolidated UK-wide guidance page for study set-up
National Contract Value Review (NCVR) process improvement
Joint UK guidance on interpretation of IR(ME)R in NHS research
Updates to RDN Portfolio Eligibility Criteria
NIHR support for 150-day study set-up for clinical trials
Guidance on detailed definitions and processes for site-level performance reporting
Bulletin: Action to enhance visibility of current research delivery set up activities in the UK
Action to enhance visibility of clinical research delivery against the UK government’s commitment to reduce the set-up time for clinical trials to less than 150 days
Webinar: Study Set-Up Plan update Progress and next steps
Study Set-Up Plan: Questions
Study Set-Up Plan: Phase 2 Completed
Bulletin: Requirement for use of the Schedule of Events Cost Attribution Tool (SoECAT) and the unmodifiable existing model Non-Commercial Agreement (mNCA) and Organisation Information Document (OID)
Study Set-Up Plan: Phase 1 Completed
Webinar: Streamlining and reform of study set-up
Study Set-Up: Trust level set up report
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Study set up: Trust level data archive
Study Set-Up: Policy Statement
UK Guidance for Study Set-Up
