Advancing Medicine Through Clinical Research
Transforming lives by connecting patients to innovative therapies.
Our Clinical Trial Process
1.Pre-Screening
2.Informed Consent
2.Informed Consent
During pre-screening, our research team gathers basic information to determine whether a study may be a good fit for you. This may include questions about your medical history, current condition, and eligibility requirements.
2.Informed Consent
2.Informed Consent
2.Informed Consent
Before any study procedures begin, you will review and sign an informed consent form. This document explains the study’s purpose, procedures, potential risks and benefits, and your rights as a participant. Our team will answer all questions to ensure you fully understand the study.
3.Screening Visit
2.Informed Consent
3.Screening Visit
At the screening visit, study-specific evaluations are performed to confirm eligibility. These may include medical exams, laboratory tests, imaging, or questionnaires, depending on the study protocol.
4.Enrollment
5.Follow-Up Visits
3.Screening Visit
If you meet all eligibility criteria, you may be enrolled in the study. Enrollment confirms your participation and allows study activities to begin according to the approved research plan.
5.Follow-Up Visits
5.Follow-Up Visits
5.Follow-Up Visits
Throughout the study, you will attend scheduled follow-up visits. During these visits, our team monitors your health, collects study data, and ensures your safety while you receive study-related care.
6.End of Study
5.Follow-Up Visits
5.Follow-Up Visits
At the end of the study, final evaluations are completed, and your participation concludes. Our team will review next steps with you and answer any remaining questions. Participation is always voluntary, and you may withdraw at any time.
