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Interagency Secretariat on Research Ethics 350 Albert Street Ottawa, ON Canada K1A 1H5 www.ger.ethique.gc.ca On behalf of the: Canadian Institutes of Health Research: http://www.cihrirsc.gc.ca Natural

Guidelines for Research on Humans The federal government and its research regulatory groups are required by law and Policy Statement 1 to develop policies in keeping with ethical guidelines for research on humans established by the National Academy of Sciences in 1991. The Natural Sciences and Engineering Research Council of Canada's statement of research principles, released January 22, 2005, states that “research will be conducted only in an atmosphere free of unacceptable risk and in the absence of unreasonable risks.” Research may also be conducted only on human subjects in accordance with the terms of the relevant Health Canada authorization and with informed consent. The statement notes that ethical guidelines for all types of research involve issues of power and authority, and the extent to which research is to be subject to human subjects protections and the principles and principles of the Helsinki Declaration for the Protection of Human Subjects. The statement provides a list of the key principles which must be taken into account when developing policy and making institutional decisions. These principles are incorporated in the NS ERC and the Departmental Policies on Research involving Human Participants that were developed in conjunction with the NS ERC Advisory Committee on the Ethics of Human Research, which is responsible for ethical review and development of NS ERC policies. The Principles cover four main considerations: 1) research projects must comply with the principles of autonomy and beneficence; 2) research ethics must be clear, objective, flexible, and accessible; 3) research subjects must be protected from exploitation, and 4) research policies and guidelines must protect the rights, autonomy, and welfare of research subjects. This document outlines the key principles that must be considered in the development and application of Federal Policies and Research Ethics and discusses them in some detail. It will be used when developing policies and guidelines related to research involving human subjects involving more than 1 person, involving human tissues or cells, or research involving any area of Health Canada-funded research. This Policy Statement was developed according to the methodology for developing public health policy of the Health Policy Manual for the Department of Human Resources and Skills Development of the Public Service of Canada. It is intended to provide guidance and information to the appropriate public policy level for the development of policies and research ethics for research involving human subjects. It is important that the public, scientists, government agencies and the media understand the policies of the federal government and its research regulatory bodies, since different jurisdictions may have different approaches to protecting human subjects. Furthermore, it is essential that policies are coordinated and are designed with this information in mind. The policies of many universities and research laboratories set out general values, but are silent on how research with human subjects might be regulated.

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What is interagency secretariat on research?

The interagency secretariat on research is a department or organization that coordinates and facilitates research efforts across multiple agencies or organizations.

Who is required to file interagency secretariat on research?

The specific entities or agencies required to file the interagency secretariat on research may vary depending on the jurisdiction or specific regulations. Typically, it includes government agencies, research institutions, and other relevant organizations involved in interagency research collaborations.

How to fill out interagency secretariat on research?

The process for filling out the interagency secretariat on research may vary depending on the specific requirements and guidelines provided by the regulatory authority. Generally, it involves providing information about the research project, collaborating agencies or organizations, funding sources, research methodologies, expected outcomes, and any other relevant details.

What is the purpose of interagency secretariat on research?

The purpose of the interagency secretariat on research is to promote collaboration and coordination among different agencies or organizations involved in research activities. It aims to streamline research efforts, share resources, avoid duplication, and maximize the impact of research outcomes.

What information must be reported on interagency secretariat on research?

The specific information that must be reported on the interagency secretariat on research may vary depending on the regulatory requirements. Generally, it includes details about the research project, participating agencies or organizations, funding sources, research methodologies, expected outcomes, timeline, and any other relevant information deemed necessary by the regulatory authority.

When is the deadline to file interagency secretariat on research in 2023?

The deadline to file the interagency secretariat on research in 2023 may vary depending on the specific regulations or guidelines provided by the regulatory authority. It is recommended to consult the official sources or regulatory documents for accurate deadline information.

What is the penalty for the late filing of interagency secretariat on research?

The penalties for the late filing of the interagency secretariat on research may vary depending on the jurisdiction and specific regulations. It can include monetary fines, delayed approvals, restrictions on future research activities, or other disciplinary actions as determined by the regulatory authority. It is advisable to consult the official regulations or seek legal advice for accurate information regarding penalties.

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