Institutional Review Board (IRB) – Practice & Procedures
Ensuring Ethical Oversight in Human Subjects Research
At Consortium Publisher – ICDTD Inc., Canada, we uphold the paramount importance of ethical review and protection of human research participants. Our publication policies rigorously comply with internationally recognized standards for ethical research oversight, particularly those governed by Institutional Review Boards (IRBs).
What is an Institutional Review Board (IRB)?
An Institutional Review Board (IRB) is an independent committee established to review, approve, and monitor research involving human subjects. The IRB’s primary role is to protect the rights, welfare, and privacy of research participants by ensuring that all research complies with ethical principles and regulatory requirements.
IRBs evaluate research protocols to ensure:
- Risks to participants are minimized and reasonable relative to anticipated benefits.
- Informed consent is obtained appropriately and documented.
- Participant confidentiality and data privacy are safeguarded.
- Vulnerable populations receive special protections.
Our IRB Policy for Published Research
To maintain the highest ethical standards, Consortium Publisher Canada requires all authors submitting manuscripts reporting human subjects research to:
- Obtain IRB Approval:
Authors must provide documented evidence of prior approval from a recognized IRB or ethics committee before conducting their research. This documentation should be included in the manuscript or supplementary materials. - Adhere to Ethical Guidelines:
Research must comply with international ethical standards, including the Declaration of Helsinki and local regulations. Studies must demonstrate that informed consent was obtained from all participants or their legal guardians. - Report IRB Details Transparently:
Manuscripts should clearly state the name of the IRB or ethics committee that approved the study, the approval reference number, and any applicable consent procedures. - Clinical Trials Registration:
In accordance with ICMJE and other regulatory bodies, all clinical trials must be registered in a publicly accessible registry prior to participant enrollment.
Editorial Procedures Regarding IRB Compliance
- Verification of Ethical Approval:
Editorial staff and peer reviewers will assess compliance with IRB requirements during manuscript evaluation. Manuscripts lacking appropriate ethical approval or documentation may be rejected or returned for clarification. - Ethical Misconduct Handling:
Any suspected breaches of ethical standards related to human subjects research will be investigated following COPE guidelines and relevant institutional policies.
Importance of IRB Compliance
Ethical oversight via IRBs is critical to:
- Safeguard human rights and dignity.
- Promote responsible conduct of research.
- Enhance the credibility and trustworthiness of published findings.
By enforcing strict IRB compliance, Consortium Publisher Canada contributes to the advancement of ethical and high-quality scientific knowledge.
Additional Resources
- Office for Human Research Protections (OHRP)
- World Medical Association – Declaration of Helsinki
- International Conference on Harmonisation (ICH) Guidelines
Contact Us
For inquiries related to ethical policies and IRB compliance, please contact us at: office@consortiumpublisher.ca
