Are you interested in becoming a trial participant? Check out the information below and learn a little more about participating in clinical studies.
Trial participant is the subject who, under personal consent or under consent of a legal guardian, accepts to be researched. Therefore, participation in clinical trials is voluntary.
The informed consent is a process by which a subject voluntarily confirms his or her willingness to participate in a particular trial, after having been informed of all aspects of the trial that are relevant to the subject’s decision to participate. The Informed Consent Form should contain, among other information: justification and objectives of the study, possible risks and benefits, existing alternative methods, and study procedures. Informed consent is documented by means of a written, signed and dated informed consent form.
Stay tuned! the trial participant has the rights to ask and clarify all questions related to the research, and it is the duty of the researchers to answer questions and clarify any doubts.
Even after consenting to participate in a trial, the participant can leave the trial at any moment, without any personal loss.
The trial participants have their identity protected and all study data are confidential.
In Brazil, the participation in clinical trials should be free, except for Phase I or bioequivalence research.
Do you want to become a trial participant? Make your registration here.