Can-Med considers the welfare, safety and comfort of the patients who volunteer and consent to participate in our clinical trials as the most important aspect of what we do. Ensuring that the experience of participating in a clinical trial to positive one is paramount and our research staff strive to be supportive, accommodating, and helpful through all stages. A volunteer or patient who, after learning all that they can about the risks, benefits, assessments and requirements associated with participating in a trial, meets the inclusion and exclusion criteria and provides informed consent, is called a Research Subject  when enrolled into the study.