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Terms of reference (Tors) for the procurement of services below the EU thresholdStudy Hindering Factors on Implementation of EPIC Principles and Impacts around Agricultural InvestmentsProject number/

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Identify the participants who will be involved in the study.

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Provide clear and comprehensive information about the study objectives, procedures, risks, benefits, and expectations to the participants.

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Who needs prior informed consent protocols?

01

Researchers conducting studies involving human participants.

02

Healthcare professionals obtaining consent for medical procedures.

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Institutions or organizations conducting research or collecting data on individuals.

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What is prior informed consent protocols?

Prior informed consent protocols are procedures that require individuals or organizations to obtain permission before sharing or using certain types of information or materials.

Who is required to file prior informed consent protocols?

Anyone who is handling sensitive information or materials that may impact others is required to file prior informed consent protocols.

How to fill out prior informed consent protocols?

Prior informed consent protocols can be filled out by providing detailed information about the information or materials being shared, the purpose of sharing, potential risks, and how consent will be obtained.

What is the purpose of prior informed consent protocols?

The purpose of prior informed consent protocols is to ensure that individuals are aware of and agree to the sharing or use of sensitive information or materials that may impact them.

What information must be reported on prior informed consent protocols?

Information that must be reported on prior informed consent protocols includes details about the information or materials being shared, the purpose of sharing, potential risks, and how consent will be obtained.

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