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As a clinical trial research subject, you also have certain responsibilities. These include: - To provide, to the best of your knowledge, accurate and complete information on all matters relating to your health.
- To ask questions when you do not understand what you have been told about the study, your care or what you are expected to do (this applies right from the time of informed consent through to the end of the study).
- To follow the study requirements to the best of your ability, including but not limited to the instructions for taking your study medication and attending study visits on time. This includes telling the research coordinator if you cannot attend a scheduled study visit with as much advance notice as possible so that it can be rescheduled.
- To express any concerns you have in your ability to follow or comply with the study requirements so that these concerns can be addressed by Dr. Pommerville and the research coordinator.
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RESEARCH SUBJECTS 
