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What We Can Do for You

Informed consent is the process of learning the key facts about a clinical trial before deciding whether or not to participate. It is also a continuing process throughout the study to provide information for participants. To help someone decide whether or not to participate, the doctors and nurses... Read More

What questions should I ask before I agree to participate in research
Regulatory and Ethics, Clinical Trial Participants, Community

We provide a information for participants on what questions to ask and what our advocates can do for you. For more information, please see the Participant Advocate Program brochure. Read More

What are my rights as a research subject/participant?
Community, Clinical Research Unit (CRU), Clinical Trial Participants, Researchers, Regulatory and Ethics

Please click on the Rights & Responsibilities for a list.  Read More

What is a research participant?
Community, Clinical Trial Participants

A research participant is someone who participates in a research study. Research involving human participants (often referred to as 'subjects') may take place in many places in and around the community. The majority of GHUCCTS-related research will take place in the Washington, DC metro area at... Read More

Our research subject advocates help ensure the rights, safety, and well-being of participants in GHUCCTS-supported research studies. Research subject advocates enhance the standard protections available for participants in clinical research through advocacy for study participants, through... Read More