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.
Literature Review Consultation
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Expert assistance in how to find high-impact, relevant studies to inform your research.
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IRB Forms Assistance
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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.
Sampling Strategy
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A sample size refers to a part of the target population that we would like to study. Selecting the appropriate sample size is important for research since it helps to generalize the findings to the entire population and improves the reliability and validity of the study. The sample size is determined by applying mathematical formulas.
