Clinical research is essential to advancing medical knowledge, helping scientists develop new ways to prevent, diagnose, and treat diseases. It involves studying people, tissue samples and data to improve healthcare outcomes.
A clinical trial is a research study that evaluates the safety and effectiveness of new treatments, screening methods, and medical interventions in humans.
Clinical trials play a crucial role in bringing FDA-approved drugs to market, ensuring new treatments are safe, effective, and better than existing options.
Our clinical trials are changing lives. Want to get involved? Explore current opportunities and see if you qualify. Reach out to our Recruitment Department today.
Clinical trials follow a structured process divided into four key phases, each designed to assess different aspects of a new treatment’s safety and effectiveness.
Tests a new drug on a small group to determine safe dosage and and confirm efficacy.
Expands testing to a larger group to monitor for adverse effects.
Tests treatment in a broader population across different regions.
Evaluates long-term effects in an extensive population after regulatory approval.
We understand that starting a clinical research journey can raise many questions. That’s why we’ve compiled answers to some of the most common inquiries to ensure transparency and clarity.
Clinical Research is the study of people, samples and data to evaluate health conditions, treatments and medical advancements. It plays a critical role in improving healthcare and developing new therapies.
Participants can vary depending on the study, but eligibility is determined by specific criteria such as age, medical history, and current health status. Our team ensures a thorough screening process for safety and suitability.
Absolutely. All our studies are conducted under strict regulatory guidelines and are overseen by experienced medical professionals to prioritize participant safety and well-being.
Clinical trials are voluntary and open to people of all ages. However, each study has specific eligibility criteria that participants must meet.
No. Health Insurance is not required to participate in a clinical trial. However, maintaining your coverage is recommended.
No. All trial-related costs are covered by study Sponsor. Participants will receive compensation for their time and effort. Transportation assistance may be provided if pre-approved by Sponsor.
Yes, participant safety is a top priority. Every trial follows strict regulatory guidelines, includes an informed consent process, and undergoes continuous monitoring.
Some studies use placebos, but this varies by trial. The research team will explain whether a placebo is involved and how the treatment assignment works before you enroll.
Discover how we can make the clinical trial process effortless for you.
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