Support in formulation of the informed consent
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An informed consent form is an ethical and legal document that must be presented to study subjects before participating in the research. The aim of this document is to provide complete information regarding the study so that participants understand what the research is and what they are agreeing to participate in. Thus, formulating the informed consent requires careful selection of the information that needs to be included in a comprehensive yet readable manner.
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Study design
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We walk you through the task of choosing the appropriate research study design from the many types of designs, each with its advantages and limitations used to collect and analyze data on variables specified in a particular research problem and deciding the most suitable methods and procedures to be used.
Transfer study proposal into IRB forms
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Your local Institutional Review Board (IRB) must first approve any research (whether it is conducted on animals or humans) that you plan to undertake. To obtain this approval you are required to complete the IRB forms and comply with their requirements. However, this can often be a delicate process and requires many documents to be submitted. Any unclear or missing information may lead to delay or rejection by the IRB. In this service, we offer guidance on how to fill the forms accurately by complying with the IRB guidelines.
