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  • Home
  • About Us
    • What we do
    • Organization Structure
    • Management Team
    • Contact Us
  • Facilities
    • Accredited Hospital Laboratory
    • Clinical Trials Pharmacy (CTP)
  • Services
  • Research Ethics
    • Ethical Principles & Guidelines
    • Clinical Research Institutional Review Board
    • IRB & FWA Registrations with OHRP
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    • Quality Assurance
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    • Audits & Inspections
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繁體 简体
  • Home

  • About Us

    • What we do

    • Organization Structure

    • Management Team

    • Contact Us

  • Facilities

    • Accredited Hospital Laboratory

    • Clinical Trials Pharmacy (CTP)

  • Services

  • Research Ethics

    • Ethical Principles & Guidelines

    • Clinical Research Institutional Review Board

      • How to Apply

      • Notes / Information for Applicants

    • IRB & FWA Registrations with OHRP

  • Quality Management

    • Quality Assurance

    • Accreditations & Recognitions

      • Laboratory Accreditation

    • Audits & Inspections

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    • News

    • Announcements

  • Strategic Collaboration

  • Links

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Clinical Research Institutional Review Board

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Clinical Research Institutional Review Board

MUST/UH IRB

At MUST/UH, clinical studies are overseen by Macau University of Science and Technology / University Hospital Clinical Research Institutional Review Board (MUST/UH IRB).

MUST/UH IRB is an independent committee, which was established in collaboration between MUST and the University Hospital (UH) in accordance with the requirements of the ICH GCP, and is governed by the two organizations through the Governance Committee (GC). It is composed of a diverse group of members, including clinical and medical expertise, non-scientific members whose primary expertise is not in any medical-related area, and independent members with no ties to either MUST or UH. Its primary goal is to protect the rights, safety, and well-being of participants in clinical studies affiliated with MUST and/or UH by providing initial and ongoing ethical and scientific evaluation of the research activities.

MUST/UH IRB operates in compliance with its written SOP and the core tenet of the Declaration of Helsinki and the ICH GCP, as well as other applicable international, national or local ethics standards or regulatory requirements

Macau University of Science and Technology / University Hospital Clinical Research Institutional Review Board (MUST/UH IRB) Secretariat: Stephanie Wong (clinicalresearchirb@must.edu.mo)

IRB Standard Operating Procedures
Application Guidelines

How to Apply

Review Fee

Notes / Information for Applicants

Forms

Ethics Review Application Form

Conflict of Interest Declaration Form for Investigators

Clinical Study Categorization Form

Amendment Form

Progress Report Form

Final Report Form

SAE Report Form

Deviation Form

IRB Meeting Dates
  • Research Ethics

    • Ethical Principles & Guidelines

    • Clinical Research Institutional Review Board

    • IRB & FWA Registrations with OHRP

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I120, Macau University of Science and Technology, Avenida Wai Long, Taipa, Macau

Operating Hours: Monday - Friday 9am - 6pm (Macau Time)

(+853) 8897-2117

ctc@must.edu.mo

Linkedin: Clinical Trials Centre, Macau University of Science and Technology

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Copyright (c) 2011-2025 Macau University of Science and Technology.

All rights reserved.