Clinical trials are research studies conducted with human participants to evaluate the safety and effectiveness of medical interventions, such as new drugs, treatments, or medical devices. These studies are a crucial step in bringing new healthcare solutions to the public, ensuring they work as intended and are safe for widespread use.
Every medication we use today exists because people like you participated in research studies. Without the dedication of participants in COVID-19 vaccine trials, we wouldn’t have the vaccines that protect us today.
Clinical Trials Ongoing worldwide
Participate annually in clinical trials
Approval of new drugs
Average compensation per clinical trials in 2023
Submit a form to express your interest to participate in clinical trials
Medical team will share information about the trial’s purpose, procedures, potential risks and benefits, and your rights as a participant. We’ll conduct vital sign checks, physical exam and blood work to confirm your health status and eligibility.
After completing the study, you’ll receive compensation for your time and effort, knowing you’ve contributed to the future of healthcare
We’ll provide preliminary information about the study, and gather information about your health and medical history.
Participation may involve physical exams, lab collection, answering questionnaires, and frequent checkups.
Yes, most clinical trials offer compensation for your time, travel, and participation. The amount depends on the specific study.
Each trial is different. Before joining, you’ll receive a clear schedule outlining what’s expected, and many studies offer flexible visit times.
No, health insurance is not required to join most clinical trials.
Results from clinical trials are typically published in scientific journals and shared with regulatory agencies. Transparency is crucial, and many trials are registered in public databases to ensure accountability.
Yes, participants can withdraw from a clinical study at any time without any consequences. It is important for participants to feel comfortable and safe throughout the research process.
Informed consent is a process that ensures participants are fully aware of the study's purpose, procedures, risks, and benefits before agreeing to participate. It is a fundamental ethical requirement in clinical research.
Participants in clinical trials are protected by informed consent, which ensures they understand the study's risks and benefits. They can withdraw from the study at any time without penalty. Regulatory bodies oversee the trials to ensure compliance with safety standards.
Participants in clinical trials may gain access to new treatments before they are widely available. They also contribute to medical research that can help others in the future. Additionally, participants receive close medical attention and monitoring.
Clinical trials are conducted under strict regulations to ensure participant safety. Before a trial begins, it must be approved by an ethics committee, and participants are monitored closely throughout the study.
Clinical trials are research studies that test how well new medical approaches work in people. They are essential for developing new treatments and improving existing ones. Each trial is designed to answer specific questions about a new treatment.
To participate in a clinical study, you can start by contacting the research team or visiting clinical trial registries. They will provide information about eligibility criteria, the study's purpose, and what participation entails.
Clinical research is a branch of healthcare science that determines the safety and effectiveness of medications, devices, diagnostic products, and treatment regimens intended for human use. It involves the participation of human subjects and is essential for advancing medical knowledge.