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Human Research Subject Rights
As a potential participant and subject in a research study, you have the following rights:
- To be told what the research study is trying to find out and what, when, where and for how long you will be involved.
- To be told what will happen to you whether any of the procedures, drugs or devices differ from what would be used in standard practice.
- To be told about any frequently occurring and/or important risks, side effects or discomfort from the things that will happen to you during the research study.
- To be told if you can expect any benefit from participating and if so what the benefit may be.
- To be told of the other choices you have and how they could be better or worse than being in the study.
- To be allowed to ask any questions and express concerns both before agreeing to be involved and at anytime during the course of the study.
- To be told what medical treatments are available if complications arise and who is responsible for payment of such services.
- To refuse to participate or change your mind about participation after the study is started without any risk to your future care.
- To receive a copy of the signed and dated informed consent document.
- To be free of pressure when deciding if you want to participate in the study.
- To know the names, positions and phone numbers of the research study investigator.
- To know how and to what extent your privacy is protected under the law.
For more information regarding Catholic Medical Center Human research Protection Program, or if you have any questions, concerns, or complaints about research conducted at Catholic Medical Center, please contact research@cmc-nh.org. Internet Resources of InterestU.S. National Institutes of HealthU.S. Department of Health and Human ServicesU.S. Food and Drug AdministrationCenter WatchOffice of Human Research Protections
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