Volunteer clinical trials singapore

Alternatively, you may leave your contact information via our Online Registration Link. What is a clinical trial?

Why participate? Find Out More! Register your interest with us today. This site is intended for use by Singapore Residents aged 21 or older. For Caregivers. Healthcare Professionals. Pre-Professional Education. NHG Residency. Medical Education Office. Nursing Resources. Central Health. About Central Health. For Central Health Partners. Central Health Resources.

For Residents. Refer a Patient. Central Health Stories. I Want To. Request an Appointment. Make a Donation. Find Medical Service. Join TTSH. The trial team will schedule several clinic visits to conduct tests and check on your well-being.

Constant communication between you and the trial team is vital to ensure your safety and proper conduct of the clinical trial. Aside from phase 1 clinical trials, studies are usually conducted on research treatments that have:. Hence there is generally a tendency for the trials to show positive results although failures due to lack of benefits or increased risks do occur late in the product development in large phase 3 studies.

In Singapore, the investigators conducting clinical trials are also specialists in the disease area being studied. You can then gain access to expert medical care as a participant in these clinical trials. At the same time, you can also get actively involved in the investigators' health care, and help others by contributing to medical research.

While clinical trials are designed to minimise the risks to all participants, but may still be demanding and time consuming. Patients are strongly encouraged to learn as much as possible about clinical trials and understand the risks associated before participating, as risks are usually specific to the drug being tested and the procedures that will be performed in each study.

A clinical trial's ethical and regulatory review help to ensure that specific aims, problems and risks or benefits are thoroughly considered and that the chosen options are scientifically sound and ethically justified. Clinical trial investigators are also required to give prospective participants complete and accurate information about what will happen during each trial. Informed consent is a process whereby investigators provide a you, a potential participant, with information about the research study.

The participant should be given ample time to consider participation in the clinical trial and have any questions addressed in a satisfactory manner before agreeing to participate. Signing the informed consent form and providing consent is not a contract.

Participants may choose to withdraw from a clinical trial at any time without any penalty, even if the clinical trial has not been completed.

The following questions may be helpful during a discussion with an investigator. Answers to the questions are provided in the informed consent document:.

You should undergo all the study procedures outlined in the informed consent form and follow the advice given by the study team. Regulatory overview. Submit a CRM notification. Good Clinical Practice Inspections. Report adverse events. Innovation Office. Conducting clinical trials. Guidance documents. Clinical Trials Register. Clinical trials statistics. A Singapore Government Agency Website. Browse Home Clinical trials.

Participating in clinical trials Understand the possible benefits, risks and your rights as a participant should you decide to participate in a clinical trial.

What is a clinical trial A clinical trial is a research study conducted to investigate new treatments, such as a new drug compound or an existing therapy, in human volunteers or research participants. How are clinical trials regulated Clinical trials in Singapore are regulated under the Health Products Act and Medicines Act and their subsidiary legislations.