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About clinical studies

What a clinical study is, what happens if you take part, and how participants are protected — written for people joining a study for the first time.

WHAT IS A CLINICAL TRIAL

What is a clinical study?

It is the process of checking whether a cosmetic or quasi-drug product is safe and effective on real people — you use the product to a set plan, and the results are measured.

Most studies at GSC Anti-Aging Lab work like this: you apply the product to your skin, then come in on set dates to be measured. They are not drug trials — there are no procedures and nothing to swallow. Every study runs strictly to a protocol approved by an institutional review board (IRB).

A researcher measuring a participant’s skin condition

How it goes

01
Find a study and apply

Pick a posting that matches you and apply online.

02
Screening

We check that you meet the criteria and let you know the outcome.

03
Visits and measurements

Come in on the agreed dates, use the product, get measured.

04
Allowance paid

Once every visit is complete, the transport allowance is paid.

IRB
Approved before anything starts
MOHW-accredited institutional review board
1–2 hrs
Fits around work or study
A quick set of measurements, then you are done
Any time
You can stop
Withdrawing carries no penalty
TRANSPORTATION ALLOWANCE

Transport allowance

The allowance depends on how many visits a study needs and how long each one takes, so it differs from posting to posting. The exact amount is on each study’s detail page.

How payment works

The allowance is paid once you have completed every scheduled visit.
Payment goes to a bank account in your own name, so we need your account details.
Payment follows the schedule announced at the end of the study; it differs from posting to posting.
If you withdraw partway through, you may be paid in part — or not at all — depending on how many visits you attended.
PARTICIPANT PROTECTION

Participant protection

Your safety and your rights come first at every stage of a study.

IRB
Institutional review board approval

Every study is reviewed by an institutional review board before it begins. The board independently checks that the protocol does not place an unreasonable burden or risk on participants.

Protocol reviewed and approved in advance
Re-review whenever the protocol changes
Periodic checks while the study runs
Consent
Full explanation, voluntary consent

Before taking part you are told the purpose, the procedure, the discomfort you can expect and the allowance, and you sign the consent form only once you understand it. You can ask anything at any point.

Written information sheet plus a verbal walkthrough
Written consent after your questions are answered
You may withdraw consent freely afterwards
Privacy
Personal data protection

The personal data we collect is used only for the study, and identifying details are stripped before the results are analysed. Everything is destroyed securely once the retention period ends.

Items, purpose and retention disclosed up front
Identifying data stored separately
Destroyed at the end of the retention period
Safety
Adverse reaction procedure

If an adverse reaction occurs during the study, use of the product stops immediately and your condition is assessed. Where necessary we arrange specialist care and follow-up.

A study coordinator you can always reach
Referral to a specialist where needed
Every reaction recorded and reported
If you have an adverse reaction

If an unexpected skin reaction or any discomfort appears during a study, contact the study coordinator straight away. We stop use of the product, assess your condition and arrange specialist care if it is needed. You may leave a study at any time, for any reason, and there is no penalty for doing so.

Study coordinator: +82-2-866-1002Weekdays 09:00–18:00 KST

See which studies are recruiting

Find a posting that matches your age and gender, and apply online in a few minutes.

See open studies