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You’ve decided to participate in a clinical research trial. You’ve connected with a representative of the study. You’ve been informed of the study’s goals, methods and process. You also signed an Informed Consent Document (ICD), confirming you understand the purpose of the study, procedures, intervention, potential risks, benefits and outcomes to participating. So, what happens next?
Part III of this educational series on research studies will explore interventional studies in more depth.
Part II of this educational series on research studies will explore observational studies in more depth.
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