FAQ

After your application is received, you undergo screening by the research team, and if you meet the eligibility criteria, you sign a consent form and join the clinical trial.

Every clinical trial is conducted only after receiving approval from the Ministry of Food and Drug Safety and passing review by the Institutional Review Board (IRB). Participant safety is the top priority, and thorough monitoring is carried out.

Yes. You may voluntarily withdraw at any time without any disadvantage. Simply notify the research team when you wish to stop.

Depending on the trial, appropriate compensation is provided for your time, transportation, and medical costs. Please check the information sheet for each individual trial for details.

Health problems related to the clinical trial are actively addressed by the research team, and the related costs are borne by the sponsor. You can find further details in the information sheet provided before participation.

Participant information is strictly managed in accordance with the Personal Information Protection Act and research ethics regulations. Identifying information is anonymized and is not used for any purpose other than research.