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Clinical Trial FAQs
A clinical trial is a research study that tests new treatments, drugs, or medical devices in human participants to evaluate their safety and effectiveness. These trials are essential for advancing medical knowledge and improving patient care.
Eligibility varies by study, but generally, participants must meet specific criteria related to age, health status, and medical history. Each trial has its own inclusion and exclusion criteria, which are detailed in the study information.
Participants can expect a thorough screening process, regular check-ins, and monitoring throughout the trial. Each study will have specific procedures, including assessments, tests, and follow-up visits, which will be clearly explained beforehand.
Participant safety is our top priority. All trials adhere to strict ethical guidelines and regulatory requirements. Before a trial begins, it is reviewed by an independent ethics committee to ensure that risks are minimized and informed consent is obtained.
Some clinical trials offer compensation for time and travel, while others do not. Details regarding compensation will be provided in the study information during the recruitment process.
Yes, participation is entirely voluntary, and you can withdraw from the trial at any time without penalty. Your decision will not affect your future medical care or your relationship with healthcare providers.
We take participant privacy seriously. All personal information is kept confidential, and data is collected and stored in compliance with relevant privacy laws and regulations. Identifiable information will not be shared without your consent.
You can stay informed about our ongoing and upcoming clinical trials by visiting our website, signing up for our newsletter, or contacting us directly for more information. We regularly update our listings to provide the latest opportunities for participation.