HRA Approvals Process
All studies led from England will require HRA approval in addition to a favourable REC opinion
SSI/SSA will no longer exist
CSP will no longer exist (from March 24th)
One form completed in IRAS (replacing separate REC and R&D forms)
Statement of Activities and Schedule of Events (plus cost attribution) completed for each site type (ie screening only, screening & treating etc)
Addition of new sites in England to existing studies will be via the HRA approval process
For more information download this ZIP file containing the schedule, form and process. You will need to save the file to your computer, you can then unzip by right clicking and select "Extract"
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