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- Sub-committees of the HRA BoardThe Board has established two sub-committees; the Audit and Risk Committee and the Pay and Remuneration Committee.
- HRA Audit and Risk Committee Manual
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- The Over-Volunteering Prevention Systems
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- National Fraud Initiative Privacy Notice
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- COVID-19 – Workplace Risk Assessment All Offices
- HRA environmental sustainability strategy – making environmental sustainability the norm
- Modern Slavery Act Statement
- News from across the HRASee more of the latest news and updates from across the HRA
- HRA Approval cohort 4 confirmedImplementation of HRA Approval continues, with the third cohort of studies incorporating all study types which exclude the first four categories of IRAS from 30 November 2015. This extends HRA Approval to a broad range of studies other than clinical trials or clinical investigations taking place in secondary care in the NHS. Early studies for this cohort have included cross-border studies with the devolved administrations, managed through compatible arrangements between the nations.
- AMS welcomes cohort 4 announcement
- HRA response to EMA consultation on the updated (ICH) E6 (R2) on good clinical practiceThe European Medicines Agency’s (EMA) recently consulted on the addendum to the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) E6 (R2) guideline on good clinical practice (GCP).
- Appointments to the Confidentiality Advisory GroupThe Confidentiality Advisory Group (CAG) is looking to appoint new members to help it deliver its existing and future functions. The CAG provides the Health Research Authority (HRA) and the Secretary of State for Health (SofS) with independent expert advice about applications for access to confidential patient information. The work of the Group is challenging, but it is also immensely rewarding. Interviews will take place on Tuesday 15, Friday 18 and Monday 21 March 2016.