Understand your rights through Informed Consent
Informed consent is an agreement between you, the study participant, and the study’s Principal Investigator (PI), designed to ensure your safety and guarantee that you fully understand the risks involved before you volunteer to participate in the research study. Medpace Clinical Pharmacology takes the informed consent process very seriously. Before the process begins, the PI and an independent oversight body known as the Institutional Review Board (IRB) must examine it closely to make sure it conforms to all FDA requirements.
Interested in learning more?
If you have questions about informed consent, review our Study Participant Information document, or contact our call center to learn more.
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