Ethics.research.ubc.ca

UBC Clinical Research Ethics General Guidance Notes

WEBInvestigators conducting clinical trials for either drugs/radiopharmaceuticals, devices or natural health products used for therapeutic purposes have special obligations that are …

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URL: https://ethics.research.ubc.ca/ore/ubc-clinical-research-ethics-general-guidance-notes

Clinical Research Ethics Office of Research Ethics

WEBPolicy Number: IORG0001050. Expiry Date: July 05, 2025. Type of Assurance: Institutional Review Board ( see details) Policy Number: IRB00001443. Expiry Date: July 05, 2025. …

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Ethics Boards Office of Research Ethics

WEBResearch Ethics Boards (REBs) are independent committees established by the University and in partnership with its affiliated hospitals and research institutes. Acting on behalf of …

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How to Obtain Ethics Approval Office of Research Ethics

WEBAny research involving human participants that is conducted at UBC facilities (including UBC-affiliated hospitals) or by persons connected to the University must be reviewed …

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Post-Approval Guidance Notes Office of Research Ethics

WEBQuestions regarding the completion of Post-Approval Activities forms preparation of an Annual Renewal submission can be directed to: BC Cancer Research Ethics Board - …

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Behavioural Research Ethics Office of Research Ethics

WEBUBC's Behavioural Research Ethics Board is responsible for reviewing behavioural or social sciences/humanities research, or research that may involve the study of patients or …

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About Human Research Ethics Office of Research Ethics

WEBNovember 2016. September 2015. Research ethics review is a process of initial and ongoing review and monitoring of research involving human participants. The process …

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Culturally Safe and Trauma-Informed Practices for …

WEB4 o At Indian Residential Schools, diseases, especially tuberculosis, played a major role in the loss of young lives due to the overcrowded conditions and lack of quality health …

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CIHR Policy Guide

WEBAs a signatory of the World Health Organization’s Joint Statement on Public Disclosure of Results from Clinical Trials, CIHR is committed to advancing open science, research …

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Online Tutorials + Training Office of Research Ethics

WEBIn addition to onsite training for UBC researchers, the Office of Research Ethics also offers access to several free, external online training resources that provide valuable …

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US Financial Conflict of Interest Office of Research Ethics

WEBUBC US FCOI tutorial (approximately 20 minutes) The presentation provides instructions for demonstrating completion of the training. A certificate of completion will be automatically …

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Participant inclusivity in research Ethnicity and race1

WEBOffice of Research Ethics #102, TEFIII, 6190 Agronomy Road Vancouver, BC V6T 1Z3 https://ethics.research.ubc.ca P:\Ethics\ORE Website\Source Files\Participant …

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Article 13.2.4 : Electronic Informed Consent

WEB1. The informed consent must contain all of the elements of informed consent required by the TCPS2 2018 guidelines and the REB consent template. 2. The electronic informed …

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Guidance Notes on Behavioural Applications Office of Research …

WEBB ehavioural Research EthicsReview at the University of British Columbia is restricted to the review of the ethical conduct of research involving humans based on a specific, …

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US Department of Health and Human Services (DHHS) …

WEBNIH Sub‐agencies. National Cancer Institute (NCI) National Eye Institute (NEI) National Heart, Lung, and Blood Institute (NHLBI) National Human Genome Research institute …

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Participant inclusivity in research Gender, sex and sexual …

WEBOffice of Research Ethics #102, TEFIII, 6190 Agronomy Road Vancouver, BC V6T 1Z3 https://ethics.research.ubc.ca August 2022 | page 1 of 3 Participant inclusivity in …

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New edition of the Tri-Council Policy Statement has been released

WEB6190 Agronomy Road. UBC Clinical Research Ethics Office. Room 210, Research Pavilion. 828 West 10th Avenue. The Secretariat on Responsible Conduct of Research has …

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UBC Research Ethics Boards

WEBJanuary 10, 2017 Page 2 The TPS2 further provides in Article 4.1 under the heading of Appropriate Inclusion, that: “When a language barrier exists between the researcher and …

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TITLE 701: Informed Consent Form

WEB4.1.3 The REB may require a separate consent form for optional procedures or substudies (e.g., tissue, blood, genetic testing or specimen banking); 4.1.4 Following the review, the …

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