On 16 April 2018, HRA Approval became HRA and Health and Care Research Wales (HCRW) Approval and now applies to all project-based research taking place in the NHS in England and Wales. We are in the process of updating our online guidance to reflect this change. For information on how to prepare and submit an application for HRA and HCRW Approval please refer to the IRAS website.
For information relating to site setup and local processes for the NHS in Wales please refer to the HCRW website.
HRA Approval brings together the assessment of governance and legal compliance, undertaken by dedicated HRA staff, with the independent ethical opinion by a Research Ethics Committee (REC) so that you only need to submit one application. It applies where the NHS organisation has a duty of care to participants, either as patients/service users or NHS staff/volunteers. References to participants include people whose data or tissue is involved in a research project.
This page provides an overview of the HRA Approval process. For detailed guidance, go to the Integrated Research Application System (IRAS).
To support you with writing and submitting your application for HRA Approval, we have also created a series of top tips, which can be found in the IRAS help section. We also recommend you visit our research planning section for help before you begin your IRAS application
If your project is led from Northern Ireland or Scotland and involves NHS/HSC sites then you will not apply to the HRA. You should apply through the appropriate NHS/HSC permission process for that lead nation. Studies with sites in Northern Ireland or Scotland are supported through existing UK-wide compatibility systems where each country accepts relevant centralised assurances from national coordinating functions to avoid duplication. Guidance is available on IRAS.
If your project is eligible for HRA Approval there are four main steps that should be completed in the following order:
When applying for HRA Approval you will need to check what supporting documents you will need to provide well in advance of when you expect to submit your application. This will avoid unnecessary delays to your application. To find out more click here.
Once you have completed the steps above, the diagram below shows you the main steps in gaining HRA Approval.
You may receive separate correspondence about your REC opinion. More detailed information on the ethical review part of HRA Approval is available.
We are currently piloting a single HRA Approval validation which incorporates both assessment and ethical review validation. Currently however you may still receive separate validation letters for the assessment and ethical review aspects of your approval.
To ensure your application is 'valid first time' then you are encouraged to read the information contained in our research planning section.
The UK Study-wide governance criteria is intended for reference and use by research sponsors and by other key parties who support researchers seeking HRA Approval.
It outlines the criteria against which research studies submitted for HRA Approval will be assessed and the standards that these studies will be expected to meet.
It is critical that sponsors understand the content of this document in order to provide appropriate advice and support to their researchers in applying for HRA Approval.
Questions or comments relating to this document and its contents should be emailed to queries@hra.nhs.uk.
Before applying for HRA Approval, a sponsor is expected to have identified potential participating sites that will be listed in the IRAS application and in most cases have discussed the project with local researchers and the research management staff supporting them. You can find contact details for Research and Development (R&D) staff at NHS organisations on the NHS R&D Forum website.
A Portfolio Application Form (PAF) is no longer required to apply for NIHR Clinical Research Network (CRN) support. To apply for NIHR CRN support you should select ‘yes’ to question 5b of the IRAS Project Filter. Key information from your IRAS submissions will then be shared with the NIHR CRN and used to assess eligibility. If HRA or HCRW Approval is not required you should contact your Local Clinical Research Network for advice on how to apply. More information is available on the NIHR website.
For non-commercial studies, you must prepare the Organisation Information Document for each type of research site in your study.
For commercial studies, you must prepare the draft template agreement you propose to use with sites and the costing template. For studies which are part of the National Institute for Health Research (NIHR) Clinical Research Network (CRN) Portfolio you must ask the lead CRN to validate the costing template, at least one week before application for HRA Approval.
We continually review and improve the approval process to ensure that it meets user needs. If you have any comments or suggestions for improvements, please feedback via the online feedback survey.
The IRAS site is where you complete your research application and can find guidance and advice specific to your application. Click here to visit the IRAS site.
