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| Who
Can Be in a Clinical Trial? |
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People
with the condition being studied as well as healthy people can participate
in a study. The FDA has very strict requirements that specify which
studies involve healthy volunteers and which studies involve patients
with the condition being studied.
The research team conducting the study will review each volunteer's
medical history and the study requirements to determine who can
participate. The team will also tell you what it means to be involved
in the study and what the risks and benefits are during the informed
consent process.
The informed consent process takes place before you join the study.
A doctor, nurse, or another person on the team will explain why
the study is being done, and what you can expect. You can ask any
questions you have about the study during this time.
Interested in participating? Fill out our
form and we will contact you. |
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