Abstract
<jats:p>The article determines the informed consent (IC) as free and voluntary will of subject ones desire to participate in clinical trial (CT) after receiving information about all aspects relevant to decision-making. The IC is documented by signing and dating the form of consent by the subject or ones legal representative as well as by the person giving explanatory talk. Despite standardized definitions, the procedure of implementation of all stages of the IC is not always properly followed and the information in medical literature is scanty.</jats:p>
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Keywords
consent
subject
ones
information
article