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Get the free Health Canada’s Research Ethics Board - Ethics Review of Research Involving Humans

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This manual provides guidance to Health Canada scientists and managers regarding departmental research involving human participants, ensuring adherence to ethical standards outlined in the Tri-Council
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How to fill out Health Canada’s Research Ethics Board - Ethics Review of Research Involving Humans

01
Collect the necessary documentation and research protocol.
02
Determine if your research involves human participants.
03
Complete the application form provided by Health Canada.
04
Include a detailed description of the research project, objectives, and methodology.
05
Address all ethical considerations, including participant consent and confidentiality.
06
Submit the application along with supporting documents to the Research Ethics Board.
07
Await feedback or request for revisions from the board, and respond promptly to any queries.
08
Once approved, keep a copy of the ethics review decision for your records.

Who needs Health Canada’s Research Ethics Board - Ethics Review of Research Involving Humans?

01
Any researcher or institution conducting studies involving human participants in Canada.
02
This includes academic researchers, industry-sponsored research, and public health studies.
03
Ethics review is required to ensure compliance with ethical standards and regulations.
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Health Canada’s Research Ethics Board (REB) is an independent committee established to ensure that research involving human participants adheres to ethical standards and guidelines, safeguarding the rights, welfare, and dignity of participants.
Researchers and institutions conducting studies involving human participants that fall under the jurisdiction of Health Canada, including clinical trials and health-related research, are required to file for an ethics review.
To fill out the application, researchers must provide detailed information about the research project, including its objectives, methodology, potential risks to participants, consent processes, and measures for participant confidentiality and data protection.
The purpose of the REB is to protect the rights and welfare of research participants, ensure ethical conduct in research, and promote public confidence in the research process by reviewing and approving research proposals.
Researchers must report information including the study design, participant recruitment methods, informed consent processes, risk assessment, data collection and analysis plans, and any funding sources or conflicts of interest.
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