Participate in Clinical Trials at FCRN
Participating in a clinical trial gives you access to new treatments before they become widely available. It also allows you to play an active role in your health care while contributing to medical advancements that can benefit others.
Benefits may include:
- Access to promising new therapies under expert medical care
- More frequent health check-ups and monitoring
- Close support and guidance from experienced clinical research professionals
- The opportunity to contribute to scientific knowledge that improves future treatments
Your Rights as a Participant
Your safety and rights are our highest priority. Before joining any study, you will receive detailed information about the trial, including potential risks and benefits.
An independent medical ethics committee oversees all our clinical trials to protect participants. You will be asked to sign an informed consent document, ensuring you understand your role and the study details.
Participation is completely voluntary. You can withdraw from the study at any time without any penalty or loss of benefits.
What to Expect When You Participate
Screening: We start by assessing your health and eligibility through questionnaires and medical exams.
Enrollment: If you qualify, we explain the study in detail and obtain your informed consent.
Study Visits: You will attend scheduled visits for assessments, treatment administration, and monitoring.
Follow-Up: Even after the study ends, we may conduct follow-ups to monitor long-term effects.
Throughout the trial, our dedicated team supports you and answers any questions.
Interested in participating?
Contact our friendly team to discuss your health, available studies, and how to begin the screening process.
We’re here to support you every step of the way.