Hra-decisiontools.org.uk

Is my study research

WEBWelcome. The aim of this decision tool is to help you decide whether or not your study is research as defined by the UK Policy Framework for Health and Social Care Research. …

Actived: 2 days ago

URL: https://hra-decisiontools.org.uk/research/

Do I need NHS Ethics approval

WEBNot all research conducted within the UK requires review by an NHS Research Ethics Committee (REC). This decision tool: You should check what other reviews or approvals …

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Consent and Participant Information Guidance

WEBWelcome to the Health Research Authority's online guidance for researchers and ethics committees on consent, and how to prepare materials to support this process. The …

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Content: Participant Information Sheet

WEBFurther guidance on health related findings is available from 'Content > PIS > Discovering health related findings'. You should also provide relevant assurance that individual …

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Do I need NHS Ethics approval

WEBThe Medical Research Council (MRC) Regulatory Support Centre worked in partnership with the Health Research Authority (HRA) to develop this tool as part of a secondment …

Category:  Medical Go Health

Is my study research

WEBThe Medical Research Council (MRC) Regulatory Support Centre worked in partnership with the Health Research Authority (HRA) to develop this tool as part of a secondment …

Category:  Medical Go Health

General Principles

WEBFor those of you who will be holding and using health information, which is a special category of personal data in GDPR(the majority of researchers producing a PIS), you …

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Principles of consent

WEBThis section of the guidance focuses on the principles of consent (both ethical and legal) and how they relate to your Participant Information Sheet (PIS). We also highlight what …

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Content: Participant Information Sheet

WEBResearch studies may reveal health related or incidental findings of which participants were unaware (clinically significant or otherwise). For help in considering the issues involved, …

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Consent and Participant Information Sheet Preparation …

WEBWelcome to the Health Research Authority's online guidance for researchers and ethics committees on consent, and how to prepare documents to support this process. In this …

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Does my project require review by a Research Ethics …

WEBAdministrations’ and the Health Research Authority’s Governance Arrangements for Research Ethics Committees (GAfREC). This document encompasses the requirements …

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Content: Consent Form

WEBA consent form should normally be used to record the consent process and a participant's agreement to take part in your study. A signature on a consent form alone does not …

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Principles of consent: Emergency

WEBPrinciples of consent: Emergency research. Emergency research poses its own set of challenges in terms of providing information about the research and obtaining consent. …

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Principles of consent: Adults Lacking Capacity (England and Wales

WEBA legal representative can be asked to give consent on behalf of an adult lacking capacity to do so themselves. Those who are able to act as a legal representative in Clinical Trials …

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Consent and Participant Information Guidance

WEBClinical Trials of Investigational Medicinal Products (CTIMPs) If a young person, aged 16 or over, is deemed not to be competent to give consent to participate in a Clinical Trial of …

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Is my study research

WEBIs my study research? To help you decide whether or not your study is research you have been re-directed to Is my study research? This tool will open in a new window when you …

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CLINICAL/ NON-FINANCIAL USUAL PRACTICE RESEARCH …

WEBMicrosoft Word - DefiningResearchTable_Oct2017. RESEARCH. SERVICE EVALUATION. CLINICAL/ NON-FINANCIAL AUDIT. USUAL PRACTICE (in public health including …

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