The volunteers are fully informed about the study and explained about the possible risks and benefits of participating in the study.
During the study, volunteers have the right to withdraw from the study at any time, regardless of the reason, but must notify the research team.
Volunteers who meet the selection criteria, when participating in a full study will be fostered and compensated for participating in taking drugs and taking blood based on the number of sampling points.The total number of sampling points is different for each study, with an average of 15 ± 3 points per study period.The bioequivalence study is usually designed in two periods.
Volunteers are given 1-3 standard meals (depending on the study).Get examination and treatment immediately when the adverse events occur. If there is a serious adverse event, the volunteer is taken to an emergency at the hospital, the rate of payment depends on the level of health insurance.
The personal information and test results will be kept confidential in the Center’s study records, volunteers have the right to not allow their real name, address … to be published in the reports on the results.magazines, newspapers.
B. Responsibility
Volunteers participate in the study voluntarily.Before joining the study, volunteers need to sign the informed consent form.
When participating in the study, volunteers must fully comply with the requirements of the study, provide accurate personal information (on request), medical history and health status before, during the study.
In case volunteers do not want to continue to participate in the study, they need to notify at least 24 hours before the official study period takes place.