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Clinical Trial

Efficacy Test for Cosmeceuticals

Clinical Trial Safety Test Efficacy Test for Cosmetics Efficacy Test for Cosmeceuticals In vitro assay Safety Test Efficacy Test

Efficacy Test for Cosmeceuticals

    • Itching alleviation test
    • This test is evaluated the changes by measuring several parameters with skin hydration and TEWL, according to MFDS guideline.

    • Test Period

      4 weeks

    • Subject

      More than 30 Subjects

    • Claim

      Help to alleviate itching by repairing skin barrier

    • Non-comedogenicity test
    • This test is to evaluate the suitability on acne-prone skin by mesuring the changes of the ance lesion and sebum output level at before and after use.

    • Test Period

      4 weeks

    • Subject

      More than 20 subjects

    • Claim

      Non-comedogenicity tested
      Suitable for acne-prone skin

    • Acne symptom relief test
    • This test is conducted in accordance with the MFDS guidelines for cosmeceuticals that advocate acne symptom relief effects, and it is especially important to select subjects who meet the severity of the selection criteria.

    • Test Period

      8 weeks

    • Subject

      More than 30 subjects * 2 Group

    • Claim

      Have an relief effect of acne skin

    • Skin wellness test by continuous UV induced skin
    • This test is evaluated the changes by measuring several parameters with hydration and wrinkle according to MFDS guideline.

    • Test Period

      12 weeks

    • Subject

      More than 30 Subjects * 2 Group

    • Claim

      Help to maintain skin wellness condition by continuous UV exposure.

    • Skin hydration test
    • This test is evaluated the significant changes by measuring skin hydration on various sites according to MFDS guideline.

    • Test Period

      12 weeks

    • Subject

      More than 30 Subjects * 2 Group

    • Claim

      Help to improve skin moisturization on human skin

    • Bluelight protection test
    • In this test, in vivo test and the in vitro test are conducted simultaneously. In vivo test determines whether blue light is protected or not and the transmittance of blue light is analyzed through the in vitro test.

    • Test Period

      6 weeks

    • Subject

      More than 20 subjects

    • Claim

      Have a bluelight protection effect

    • Sweat resistance test
    • This test is performed in accordance with the test method developed by DERMAPRO to confirm the effect of UV protection due to sweat (Running conditions).

    • Test Period

      8 weeks

    • Subject

      More than 12 subjects

    • Claim

      Activity sweat proof

    • Sweat resistance test
    • This test is performed in accordance with the test method developed by DERMAPRO to confirm the effect of UV protection due to sweat (Sauna conditions).

    • Test Period

      8 weeks

    • Subject

      More than 12 subjects

    • Claim

      Sweat resistant or
      Very sweat resistant

    • Water resistance test
    • This test is conducted in accordance with the latest international test methods such as the MFDS Guidelines, Cosmetics Europe, ISO18861:2020 and ISO16217:2020 for sunscreen cosmetics that advocate water resistance effect.

    • Test Period

      8 weeks

    • Subject

      More than 12 subjects

    • Claim

      Water resistant or
      Very water resistant

    • Sun protection factor test
    • This test is conducted in accordance with the latest international test methods such as the MFDS Guidelines, ISO24444:2019, JCIA and FDA for sunscreen cosmetics that advocate UVB protection effect.

    • Test Period

      6 weeks

    • Subject

      More than 12 subjects

    • Claim

      SPF value

    • Protection factor of UVA test
    • This test is conducted in accordance with the latest international test methods such as the MFDS Guidelines, ISO24442:2022 and JCIA for sunscreen cosmetics that advocate UVA protection effect.

    • Test Period

      6 weeks

    • Subject

      More than 12 subjects

    • Claim

      PFA value or +++,++++

    • Hair loss alleviation test
    • This test analyzes the total hair counts of 1 cm2 and visual assessment by dermatologists in accordance with the MFDS guidelines for functional cosmetics that advocate the effect of relieving hair loss symptoms.
      Since the automation program analysis gene

    • Test Period

      24 weeks

    • Subject

      More than 20 subjects * 2 Group

    • Claim

      Have a relief effect on hair loss