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| A Guide for Clinical Audit, Research and Service Review — An educational toolkit designed to help staff differentiate between clinical audit, research and service review activities | |
| Type: Guide Author: HQIP Keywords: QI, Quality Improvement, research, service evaluation, research definitions, research categories Link Reference: 697 Click here to access the resource |
| A guide to reporting protocols of pilot & feasibility trials | |
| Type: Guide Author: Lehana Thabane and Gillian Lancaster Keywords: reporting, transparency, protocols, feasibility trials, Clinical Trials, pilot trials Link Reference: 760 Click here to access the resource |
| A joint statement setting out the legal and ethical requirements for seeking and documenting consent using electronic methods. | |
| Type: Guidance Author: HRA and MHRA Keywords: consent, e-consent, electronic consent, clinical trials, GCP, e-systems, compliance, validated systems, e-signatures, ethics, research ethics Link Reference: 754 Click here to access the resource |
| A new pathway for the regulation and governance of research (2011) | |
| Type: Report Author: Academy of Medical Sciences Keywords: History, Governance, Regulation, Policy, Context Link Reference: 246 Click here to access the resource |
| A new strategy for the changing world of health and social care – CQC’s strategy from 2021 | |
| Type: Example Strategy document Author: CQC Keywords: understanding the landscape, regulation, innovation, research, strategy Link Reference: 19780 Click here to access the resource |