Company

Corederm Co., Ltd. specializes in conducting skin clinical trials for cosmetics, household goods, over-the-counter drugs, health functional foods, and beauty devices.

Vision

Corederm Skin Clinical Trial Institute, Inc., is a human application testing institute specializing in skin clinical trials for cosmetics, functional cosmetics, over-the-counter drugs, health functional foods, and beauty devices.
We offer a variety of clinical trial services through collaboration between our medical team, comprised of experienced dermatologists, ophthalmologists, and dentists, and our skin clinical evaluation R&D team.
Corederm Skin Clinical Trial Institute, Inc., provides total solutions that meet our customers' needs, guided by the following philosophy:

Management Philosophy

Clinical trials are studies conducted on human subjects to predict the effectiveness and value of interventions by comparing them with a control group.
Interventions include prevention, diagnosis, treatment, and management, drugs, plans, prescriptions, and methods. A well-planned and executed clinical trial is a powerful experimental technique for evaluating the effectiveness of interventions.

All clinical trials conducted at Corederm Skin Clinical Trial Institute are conducted in compliance with the ethical standards based on the Declaration of Helsinki and the human application test guidelines of the Ministry of Food and Drug Safety.

01

Reliability in keeping promises and regulations

02

Upright and transparent professional ethics

03

Openness of communicating with an open mind

Professionalism

  • All treatments and decisions made for research subjects are under the responsibility of the physician.
  • All investigators involved in human clinical trials have received education, training, and professional experience in their respective fields of expertise.

Ethics

  • The rights, safety, and welfare of all research subjects participating in all trials are given top priority.
  • Voluntary consent for clinical trial participation is obtained from all research subjects prior to participation in human clinical trials. All records regarding the subjects' identities are kept confidential.

Standardization

  • Human application trials are designed with scientific validity, and the plans and reports are clearly and thoroughly described.
  • Human application trial-related information is recorded, processed, and preserved to enable accurate reporting, interpretation, and verification.