Frequently Asked Questions

Clinical research is a scientific study conducted with human participants to investigate the safety, efficacy, and effectiveness of medical interventions, treatments, or therapies. It aims to generate valuable evidence that guides medical decision-making, advances medical knowledge, and improves patient care.

 Clinical research involves the participation of individuals who meet specific criteria, such as patients with a particular medical condition or healthy volunteers. Participants may vary in age, gender, health status, and other factors depending on the study's objectives and target population.

Yes, all participants are compensated for their time and travel for participating in a clinical trial.

All study procedures are covered by the pharmaceutical with no cost to you nor your insurance.

Clinical research studies can include clinical trials, observational studies, epidemiological studies, and other research methodologies. Clinical trials are divided into phases (Phase 1, 2, 3, and sometimes Phase 4) and involve investigating the safety, dosage, effectiveness, and side effects of a medical intervention.

Participants in clinical research are protected through informed consent, a process that ensures they have a clear understanding of the study's purpose, procedures, potential risks, and benefits before deciding to participate. Additionally, research studies must follow ethical guidelines, obtain approval from research ethics committees, and adhere to regulatory requirements to ensure participant safety, privacy, and rights.

Yes, participation in clinical research is entirely voluntary. Individuals have the right to choose whether or not to participate in a study after considering the study details, potential risks and benefits, and consulting with healthcare providers or family members.

Yes, participants have the right to withdraw from a clinical research study at any time, without providing a reason. Researchers and study coordinators will respect the participant's decision and ensure their ongoing care and safety.

Clinical research studies may involve some risks, such as potential side effects from experimental treatments or procedures. However, researchers take extensive precautions to minimize risks and closely monitor participants throughout the study. The potential benefits and risks of a study should be thoroughly explained during the informed consent process to help participants make an informed decision.