Volunteer protection is my priority.
Dr. Hong is the chief supervisor of a clinical trial. He designs research protocols addressing study objectives and submits protocols to research ethics committees and regulatory bodies for approval. Before a trial begins, he explains to volunteers about the clinical study, the procedures, their rights and potential risks. During the trial period, Dr. Hong closely monitors the volunteers. In case of an adverse event is observed, he will immediately perform medical evaluation, provide appropriate treatment, and report the events to relevant authorities.
I care about volunteers' needs.
Ceci is a research nurse. She assists the investigators to conduct clinical trials and offers the best care to the volunteers. Ceci ensures research protocols are strictly followed whilst undertaking clinical trial procedures and collecting blood or urine specimens from volunteers. In case of medical emergency, she will inform the investigator immediately and arrange for medical assessments.
I protect volunteers' rights, safety and well-being by detailed evaluation of clinical studies.
Tak is a member of the research ethics committee (REC). He reviews clinical trial documents submitted by investigators, including study protocols, informed consent forms and such, to ensure that trial designs are scientifically valid and align with the prevailing ethical standards. The ultimate goal is to safeguard the rights, safety and well-being of volunteers.
I practise good laboratory management to safeguard research data integrity.
Jun is a laboratory technician. His laboratory analyzes blood or urine samples collected from volunteers for safety, efficacy and pharmacology assessments. Testing reports are issued by the laboratory to research teams for further analysis and evaluation.
My contribution today, our better health tomorrow.
Sammy is a volunteer, the most important role in clinical trials. She devotes her time for the advancement of medical technologies. Sammi is first informed by the investigator of the arrangements of a trial and the potential risks. After signing the informed consent form, the investigator and research nurse perform examinations on and collect blood samples from Sammi to confirm her eligibility to enroll in the trial. During the trial period, Sammi visits the study centre regularly to undergo the required study procedures and examinations.
I manage your drugs, you can use with trust.
Yuki is a research pharmacist. She manages study drugs, including drug storage, preparation and dispensing. In particular, she prepares and dispenses study drugs in accordance with research protocols and investigators’ prescriptions to ensure that study drugs are correctly dispensed to and used safely by volunteers.