The International Livestock Research Institute (ILRI) is committed to promotion of the highest standards for research by ensuring both ethical and legal obligations are met. The Environment and Occupational Health and Safety (EOHS) unit facilitates ILRI's research compliance programs by providing oversight and coordination of research compliance related activities including ethics (animal and human) approvals, biosafety and or biosecurity related approvals, application for research licenses and permissions for moving research materials.

It is expected that all persons involved in research (including institutional officials, directors, principal investigators, staff, collaborators and students) clearly understand and meet their responsibilities in relation to research compliance when engaged in research activities.
ILRI has established specific research compliance committees that review and approve research related activities. The committees cover areas that include human ethics, animal ethics and welfare, and biosafety and biosecurity. These committees are:

• Institutional Animal Care and Use Committee (animal ethics)
• Institutional Biosafety Committee (biosafety and biosecurity)
• Institutional Research Ethics Committee (human ethics)

ILRI has established The Institutional Animal Care and Use Committee (IACUC) to review and approve all activities that involve use of animals. The use of animals is defined as any activity involving vertebrate animals in which the natural lifestyle or movements of the animals is materially altered. Use of animal carcasses, tissues, and fluids obtained specifically for research or testing purposes are subject to review according to applicable regulations and may be determined to be 'use of animals'.

ILRI IACUC’s mandate includes review of all research projects to be conducted at ILRI or any other premises or field sites for which ILRI is responsible, and also to review any research projects which are led by ILRI scientists or have involvement of ILRI scientists as part of their duties as an ILRI employee. This is irrespective of the funding agency or the place of research and irrespective of the scope or nature of the research. Where the research proposal is being led by another institute then ILRI approval will not be granted unless the proposal has been approved by the relevant committee of the lead organization. The IACUC’s responsibility also involves carrying out post approval monitoring of research projects or activities and undertaking periodic review of its own policies, procedures and performance.

Refer to the ILRI animal care and use operational guidelines (cgiar.org) for more information regarding how ILRI IACUC operates. You can also write to ILRI IACUC for further information required and or report any concerns regarding the use of animals in research to ILRIResearchCompliance@cgiar.org

ILRI IACUC released the second edition of the ILRI animal care and use manual (cgiar.org). As with the previous edition, it serves as a resource and guide to all personnel working with animals and presents standard operating procedures (SOPs) that are currently in use at ILRI. They are significant in number and have been broken down into the 12+ species worked with at different ILRI locations.

Application Process
For details on how to apply to ILRI IACUC for review and approval through the ILRI Research compliance portal, download ‘How to make an application’. 

To apply for approval of your animal use activity, download, complete and submit the IACUC application Form (cgiar.org) together with other required documents to ILRIResearchCompliance@cgiar.org or through the ILRI research compliance portal.

To apply for renewal of your approval, download, complete and submit the IACUC renewal of approval form (cgiar.org) to ILRIResearchCompliance@cgiar.org or through the ILRI research compliance portal.

To apply for approval of minor amendments, download, complete and submit the IACUC Minor Amendment Form (cgiar.org) to ILRIResearchCompliance@cgiar.org or through the ILRI research compliance portal.

To submit project close report, download, complete and submit the IACUC PI Report Back Form (cgiar.org) to ILRIResearchCompliance@cgiar.org 

The Institutional Biosafety Committee is responsible for approval of all ILRI research (by ILRI principal investigators or research staff or a system component with a signed Memorandum of Understanding  with ILRI) that involves the use of biological agents. 

Projects using non-pathogenic biological agents or those categorized as Biosafety Level 1 only need to notify the committee. The biosafety program team reviews applications and gives feedback to applicants within five working days and notifies the committee.

Research that involves any of the agents listed below must be approved by the committee before the work starts:

• Pathogens and potential pathogens of humans, animals, or plants
• Materials potentially containing human pathogens (including human blood, tissue and cell lines; non-human primate blood, tissue and cell lines)
• Recombinant DNA (and RNA), including creation or use of transgenic plants and animals
• Any material requiring an import or export license or a permit

The committee is responsible for reviewing and approving biological research projects and oversees ILRI's biosafety program. The committee coordinates application procedures for biological research to ensure that research personnel have adequate occupational health monitoring and training in safe work practices, including how to handle emergencies and use of personal protective equipment.

As well as considering new proposed activities, the committee also reviews ongoing research for changes which would necessitate use of different procedures. The committee ensures that laboratory activities are planned and executed so that every reasonable precaution is taken to protect the health and safety of employees, visiting scientists, students and the public and to prevent damage to property and the environment. The committee carries out these functions in accordance with national and international laws.

ILRI has established Institutional Research Ethics Committee (IREC) to review and consider for approval all ILRI research proposals with a view to safeguard the dignity, rights, safety and well-being of all actual and potential research participants and the wider community. The ILRI IREC ensures that the cardinal principles of research ethics (autonomy, beneficence, non-maleficence and justice) are followed in planning, conduct and reporting of ILRI research. 

The mandate of the ILRI IREC is to review all research projects to be conducted at ILRI or any other premises or field sites for which ILRI is responsible, and also to review any research projects which are led by ILRI scientists or have involvement of ILRI scientists as part of their duties as an ILRI employee. This is irrespective of the funding agency or the place of research and irrespective of the scope or nature of the research. Where the research proposal is being led by another institute then ILRI approval will not be granted unless the proposal has been approved by the research ethics committee of the lead organization. 

Refer to the ILRI IREC Operational Guidelines (cgiar.org) for more information regarding how ILRI IREC operates. You can also write to ILRI IREC for more information you may require and or report any concerns to ILRIResearchCompliance@cgiar.org

Application Process

For details on how to apply to ILRI IREC for review and approval through the ILRI Research compliance portal, download ‘How to make an application (cgiar.org)’. 

To apply to ILRI IREC, download, complete and submit the IREC Application Form (cgiar.org) together with other required documents to ILRIResearchCompliance@cgiar.org or through the ILRI research compliance portal.

To apply for renewal of ILRI IREC approval, download, complete and submit the IREC Renewal of Approval Form (cgiar.org) to ILRIResearchCompliance@cgiar.org or through the ILRI research compliance portal.

To apply for approval for minor amendments, download, complete and submit the IREC Minor Amendment Form (cgiar.org) to ILRIResearchCompliance@cgiar.org or through the ILRI research compliance portal.

To apply for import or export permit, download, complete and submit Movement (shipping) of research materials form (cgiar.org) to ILRIResearchCompliance@cgiar.org or through the ILRI research compliance portal.