NSW Population and Health Services Research Ethics Committee

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This committee has responsibility for ethical reviews of any research involving data and statistics held by NSW Health and the Institute.

Research projects reviewed by this committee may include:

  • Population health research utilising data from the NSW Central Cancer Registry, the NSW Pap Test Registry, BreastScreen Registry, and other data and information collected, held and/or managed by the Cancer Institute NSW.
  • Population health research utilising data from the NSW Health Inpatient Statistics Collection, the NSW Midwives Data Collection, the NSW Emergency Department Data Collection, and other data and information collected, held and/or managed by NSW Health.
  • Research involving the linkage of a population health data collection owned and/or managed by NSW Health or the Cancer Institute NSW, with other data collections.

Submitting Proposals

Application forms are available via Online Forms, the national system that enables users to complete their applications for research electronically.

For information on the required documentation for submissions to the NSW Population & Health Services Research Ethics Committee, please refer to the Submission Checklist. Please include a copy of this checklist with your application.

  1. Applicants must email a copy of the submission checklist, the application form and all support documentation to: ethics@cancerinstitute.org.au
  2. Please send in hard copy, one (1) copy of all documentation (with original signatures), and eight (8) copies:
  • Via Post:

    Ethics Coordinator
    Cancer Institute NSW
    PO Box 41
    Alexandria NSW 1435

  • In Person:

    Ethics Coordinator
    Cancer Institute NSW
    Australian Technology Park
    Level 9, 8 Central Avenue
    Eveleigh, NSW 2015

Please note: applications will not progress to a committee review if a soft copy (via email) is not provided with the required number of hard copies. Uncollated documents will not be accepted.

2012 meeting dates

The NSW Population & Health Services Research Ethics Committee meets on a monthly basis. Submission closing dates for applications are 11 working days prior to the next meeting. This allows for independent scientific review.

Meeting Date Submission Closing Date
16th February 1st February
15th March 29th February
19th April 4th April
17th May 2nd May
21st June 6th June
19th July 4th July
16th August 1st August
20th September 5th September
18th October 3rd October
15th November 31st October
20th December 5th December

Data governance

Proposals involving access to data held or managed by the either the Cancer Institute NSW, including the Central Cancer Registry, the Pap Test Registry, Breast Screen NSW, or the Cervical Screening Program, or the NSW Department of Health must be reviewed by the relevant Data Custodian before applying to the Ethics Committee.

Researchers are required to complete a Data Request Form NSW CCR only and submit this to the relevant data custodian for review.

Data custodians are required to sign off on all requests for data from registries owned or managed by NSW Health or the Institute. The Data Custodian Sign Off form must be included with the application form.

The Ethics Committee will not review research proposals unless researchers have contacted the relevant data custodian, and an assessment of data governance issues has been started. For further information about this process, please refer to the Cancer Institute NSW Data Governance policy.

While the Ethics Committee will determine the ethical acceptability of such proposals, the authority to release data lies with the data custodian of the particular data collection, and Director-General of NSW Health or his/her delegate for individually identified data.

Committee members

The current members of the NSW Population and Health Services Research Ethics Committee include experts in research and clinical care, lay members and religious representatives.

The NSW Population & Health Services Research Ethics Committee has been constituted in accordance with the National Health and Medical Research Council's National Statement on Ethical Conduct in Human Research (2007).

Member NHMRC Category
Prof Richard Madden Chairperson
Dr Sallie Pearson (Deputy Chair) Research Experience
Ms Patricia Kenny Research Experience
Dr Alys Havard Research Experience
Dr Deborah Loxton Research Experience
Dr Lucy Burns Research Experience
Dr Natasha Nassar Research Experience
Prof Deborah Black Research Experience
Prof Kathryn Refshauge Professional Care
Dr Ingrid Evans Biostatistician
Mr Jason Bentley Biostatistician
Dr Jo Mitchell Chief Health Officer Nominee
Dr Louise Fitzgerald Lay Member
Mr Raymond Tong Lay Member
Ms Rachel Williams Lay Member
Dr Isabel Karpin Legal Member
Mr Geoffrey Bloom Legal Member
Pastor Rachael Goth Religious Member
Rabbi Jeffrey Cohen Religious Member
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