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The Unit is headed by a Director of Research, assisted by an Administrator, Clinical Research Co-ordinators, Research Assistants, Study Coordinators and an Administrative Assistant. For any enquiries, please contact Elaine Pek Conditions Which Apply To Research Conducted in IMH/WH The Principal Investigator (PI) must be a staff from IMH/WH. You have the options of applying for grants: - Applications are reviewed on a monthly basis and so, must be submitted 1 week before the monthly Clinical Research Committee (CRC) meeting. The following procedures are applicable to all investigators in IMH and those from other institutions seeking to undertake research in IMH/WH. If the proposed study is a collaboration between IMH and other centres, the PI of the other centre must produce documentation that the protocol has been reviewed and approved by the PI's supervisor or Departmental Representative. For studies which involve recruitment of our patients or staff as research subjects, a Co-PI must be one of the Institute staff. All research projects conducted in IMH and those conducted by IMH staff in or outside IMH need approval by the IMH Clinical Research Committee (CRC) and ethics approval from the Domain Specific Review Board (DSRB). Application forms for review by IMH CRC can be obtained from the Secretary, CRC Or from DSRB website on the NHG
Internet 5. The PI must get the approval of the Chief/Head of Department before submitting the results of the study to any journal for the purpose of publication. A copy of the published article must be sent to the Research Unit. Application For Research Project Funding Ethical Considerations In Research Ethical considerations of research guidelines DSRB application form download Investigators will receive a notification from the DSRB upon approval. Projects can only commence after DSRB approval. Research Guidelines for Investigators Evaluation Of Study Protocol Guidelines With Regard To Collaborations With Pharmaceutical
Companies
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