Guidelines for MUST/UH IRB Application

First Application Procedure

Provide details in the Application Form

    1. Ethics Review Application Form (please submit in English, word file. Only applicable for application form) 

Provide all the key documents by providing the key documents a specific Document Name with Version No. and Date ( e.g. Study Protocol_V01_dated16May2022 )

    2. Conflict of Interest Declaration Form for Investigators

    3. Clinical Study Categorization Form

    4. Study protocol 

        Special Remind:

        a. Compensation to Participants

             - please specify if the patients were charged for procedures while participating in a study

             - Please specify if participants will receive any payment for their visit or participation in detail

        b. Collecting Samples

             - Please specify if payment is involved for subjects and if it involves collecting samples, please provide in detail

             - If a study wants to use previously collected samples for research, a new consent is required

    5. Informed consent form and/or participants information sheet

    6. Principal Investigator's and Physician's CV(Clinical/clinical research related) 

 IF APPLICABLE

    7. Payment Record of Crossed cheque/bank draft

    8. Participant’s recruitment materials

    9. Documents/materials for use by participants in the study (e.g. participant-administered questionnaire)

Email to IRB Secretariat

    10. Submit your digital application with Covering Submission Letter to clinicalresearchirb@must.edu.mo 

    11. Send in one hard-copy set (with the required “Original Signatures”) to IRB Office (MUST Campus I120) for initial         checking. 

NOTE:

** Please be advised that only applications relating to clinical research in Macau will be accepted.

** Please sign and scan any forms that require your signature and attach them to the PDF. Please note that digital signatures are not accepted. Thank you.