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1Proven Systems and Comprehensive Clinical Trial Capabilities

The Clinical Trial Center at Central Hospital is fully qualified in accordance with Article 34 of the Pharmaceutical Affairs Act regarding the designation of clinical trial institutions. The center conducts a broad range of clinical studies, including Phase I through Phase IV trials, supported by established systems and experienced research professionals.

Areas of Clinical Research

  • Bioequivalence (BE) Studies

  • Phase I Clinical Trials (Clinical Pharmacology Studies)

  • Phase II Clinical Trials (Therapeutic Exploratory Studies)

  • Phase III Clinical Trials (Therapeutic Confirmatory Studies)

  • Phase IV Clinical Trials (Post-Marketing Studies)

  • Human Application Studies

  • Exploratory Clinical Studies

2Robust Clinical Trial Infrastructure

  • Facilities and Systems Meeting Domestic and International Standards

    The Clinical Trial Center operates in compliance with international Good Clinical Practice (GCP) standards and guidelines established by the Ministry of Food and Drug Safety (MFDS), supported by advanced equipment and a systematic operational framework.

  • Facilities

    - 76-bed Clinical Research Unit
    - Specimen Processing and Storage Room
    - Institutional Review Board (IRB) Office
    - Education and Training Room
    - Document Archive
    - Physical Examination Room
    - Participant Interview Room
    - Principal Investigator Office
    - Sub-Investigator Office
    - Investigational Product Storage Room
    - Quality Assurance (QA) Office
    - Clinical Research Coordinator (CRC) Office
    - Monitoring Room

  • Dedicated Research Personnel

    - Clinical trial investigators, pharmacologists, and study physicians
    - Experienced research pharmacists specializing in bioequivalence studies
    - CRC team with more than 10 years of clinical trial experience
    - Specialized support staff including QA personnel, administrators, medical writers, and document management officers

3Customized Support for Sponsors and Participants

  • Central Hospital's Clinical Trial Center is committed to conducting scientific and ethical research through a well-established management system that prioritizes participant safety, rights, and welfare while ensuring reliable and high-quality clinical trial outcomes.
    Through close collaboration among investigators, coordinators, pharmacists, and support personnel, the center provides efficient study management and participant-centered care throughout every stage of the clinical trial process.

Medical Team

Our Medical Team

Last Updated :2026-07-20

  • 김민기

    Center Director

    Kim Min Ki

    Laboratory Medicine

    Clinical chemistry, blood gas analysis, point-of-care testing (POCT), blood banking, urinalysis and microscopy, fecal occult blood testing, internal and external quality control, laboratory accreditation, therapeutic drug monitoring (TDM), and pharmacokinetics

  • 신인철

    Professor

    Sin Inchul

    Clinical Trial Center

    clinical pharmacology, bioethics

  • 채수용

    Chief of the Clinical Trial Center

    Chae Sooyong

    Clinical Trial Center

    Clinical research management