Hra-decisiontools.org.uk

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 …

Actived: 5 days ago

URL: https://www.hra-decisiontools.org.uk/consent/

General Principles

WebPrinciples of consent: General principles and role of Participant Information Sheets. For consent to be considered both legal and ethical it must be: Given by a person with …

Category: Health Go Health

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. …

Category: Health Go Health

Consent and Participant Information Sheet Preparation …

WebConsent & Participant Information Sheet Preparation Guidance released March 3. rd. 2014 5 . Welcome . Welcome to the Health Research Authority's online guidance for …

Category: Health Go Health

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 …

Category: Health 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 to the …

Category: Medical Go Health

Content: Participant Information Sheet

WebBefore anyone decides if they wish to take part in your research study, they need to be made aware of what would be involved. You should make clear which interventions are …

Category: Health Go Health

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 …

Category: Health Go Health

Do I need NHS Ethics approval

WebSeptember 2018 – this tool has been updated to align with revision of Governance Arrangements for Research Ethics Committees. This tool was developed by the HRA, in …

Category: Health Go Health

Content: Participant Information Sheet

WebYou should tell potential participants how their confidentiality will be safeguarded during and after the study. You may wish to tell potential participants how your procedures for …

Category: Health Go Health

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 …

Category: Health Go Health

Does my project require review by a Research Ethics …

Web‘Does my project require review by a Research Ethics Committee?’ V 2.0 2

Category: Health Go Health

Principles of consent: Children and Young People (Scotland)

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 an …

Category: Health Go Health

CLINICAL/ NON-FINANCIAL USUAL PRACTICE RESEARCH …

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

Category: Health Go Health

Participant Information Sheet (PIS) Template

WebParticipant Information Sheet (PIS) Template. This is not offered as a rigid template, but rather a flexible framework. We have suggested sub-headings which you may decide are …

Category: Health Go Health