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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
Study Set-Up: Latest news
Espandi sezione Study Set-Up: Latest news
Bulletin: Action to enhance visibility of current research delivery set up activities in the UK
Webinar: Streamlining and reform of study set-up
Study Set-Up Plan: Phase 1 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 2 Completed
Study Set-Up Plan: Questions
Webinar: Study Set-Up Plan update Progress and next steps
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
NIHR support for 150-day study set-up for clinical trials
Guidance on interpretation of IR(ME)R in NHS research
Updates to RDN Portfolio Eligibility Criteria
Study Set-Up: Trust level set up report
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Study Set-up
Study Set-Up: Latest news
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Bulletin: Action to enhance visibility of current research delivery set up activities in the UK
Webinar: Streamlining and reform of study set-up
Study Set-Up Plan: Phase 1 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 2 Completed
Study Set-Up Plan: Questions
Webinar: Study Set-Up Plan update Progress and next steps
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
NIHR support for 150-day study set-up for clinical trials
Guidance on interpretation of IR(ME)R in NHS research
Updates to RDN Portfolio Eligibility Criteria
Study Set-Up: Trust level set up report
Espandi sezione Study Set-Up: Trust level set up report
Study set up: Trust level data archive
Study Set-Up: Policy Statement