Subject / Study Participant

An individual who participates voluntarily in a clinical trial who is expected to receive the investigational product(s) or a control.

Subjects may be healthy volunteers or patients with a specific conditiondepending on the study design and objectives. After giving their informed consent (or, in cases where consent cannot be given, through a legally authorized representative), a study participant is enrolled by the investigator who is responsible for their wellbeing, health and rights in regard to the clinical study conduct.