Access forms, templates and guidelines
Researchers must ensure their projects comply with all relevant policies, legislation and guidelines.
In preparing your application, refer to the following resources:
Macquarie University templates:
- MQ Research Protocol (detailed) or HREA project description
- MQ guidelines for creating PICFs – Guide to creating participant information and consent forms (PICF).
- MFA (Multi-Factor Authentication) guide for FoRA users – Guide for applicants and HREC and Subcommittee members.
Applicant Guides for Forms for Research Applications (FoRA)
All applications must be submitted via Forms for Research Applications (FoRA). For more information about this system, what form to use, how to submit an application refer to the following FoRA user guides:
FoRA - Human Research Ethic Applications (HREA) Applicant Guide
FoRA - Externally Approved Applications (EAEF) Applicant Guide
FoRA - HREA Integrated Data Management Plan (DMP) Applicant Guide
FoRA - HREA Risk Assessment (RA) Applicant Guide - (RA guide includes links to the HREA and DMP guides)
To help you navigate your way through the new Risk Assessment and DMP filter questions of the HREA, please refer to the how-to-guides and instructional videos:
- Risk Assessment Section
- Data Management Section
Macquarie University policies:
NSW legislation:
- Anatomy Act 1977
- Human Tissue Act 1983
- Privacy and Personal Information Protection Act 1998 No. 133
- Commission for Children and Young People Act 1998
- State Records Act 1998
- Health Records and Information Privacy Act 2002
Australia and international:
- National Statement on Ethical Conduct in Human Research
- Australian Code for the Conduct of Responsible Research
- NHMRC Participant Reimbursement PolicyMacquarie University Systems and Data Management Guidelines
- Challenging Ethical Issues in Contemporary Research on Human Beings
- Australian Electoral Commission Supply of Elector Information for use in Medical Research
- Statement on Consumer and Community Participation in Health and Medical Research
- World Medical Association Declaration of Helsinki (8th revision)
- Oral History Association of Australia Guidelines of Ethical Practice 2007
- Ethical Conduct in research with Aboriginal and Torres Strait Islander Peoples and communities: Guidelines for researchers and stakeholders
- Keeping research on track II
- Australian Institute of Aboriginal and Torres Strait Islander Studies (AIATSIS) Code of Ethics
- Other AIATSIS guides and resources
- Values and Ethics – Guidelines for Ethical Conduct in Aboriginal and Torres Strait Islander Health Research
- Aboriginal Health and Medical Research Council (AHMRC)
Depending on the age of the child and their capacity to understand the research, consent from children can be obtained in the following ways:
- verbally, and recorded in writing, audio recording or video recording
- using simple words or pictures to convey the information, in paper format or electronically
- using a child-friendly version of a parent information and consent form, written in age-appropriate language.
The following reference article discussing the ethical issues concerning consenting children may also be useful:
Recruiting participants from schools
Research in New South Wales state schools requires approval from the NSW Department of Education and Communities via the State Education Research Application Process (SERAP).
All researchers submitting a SERAP form must obtain insurance sign-off from Macquarie University’s Risk and Assurance Unit. This sign-off is obtained via the ‘SERAP-Risk & Assurance Checklist’ form, which is available online in the Forms for Research Applications (FoRA) system.
Research in:
- other states’ public schools or state education sites require approval from the relevant state government Department of Education eg if you want to conduct research involving QLD department sites and/or data, you must submit an application via the Queensland Education Research Inventory (QERI)
- Catholic schools require approval from the relevant Catholic Education Office Diocese
- independent/private schools require approval from the principal.
Download guidelines for collecting demographic data.
This document outlines the wording we would recommend for diversity demographic questions based on current expert advice. These could be included in data systems, forms and surveys. It may not be necessary to include all these questions – it is always important to consider why you are collecting data and how it will be used.
For more information on collecting, interpreting and acting on diversity data, contact:
- workplacediversityinclusion@mq.edu.au for questions relating to staff data
- respect@mq.edu.au for questions relating to student data.
Whether or not you can use data collected or held by a third party depends on:
- the type of data being collected
- the purpose for which it was collected
- what consent was obtained from participants at the time of initial data collection
- how it is to be used in your research.
Sharing data can be complex and is subject to the relevant national and state legislation. You should contact the Ethics Secretariat for tailored assistance, after consulting the following guidelines, policies and legislation:
- Chapter 2.3: Qualifying and Waiving Consent, from the National Statement on Ethical Conduct in Human Research
- Office of the Australian Information Commissioner (OAIC)
- Health Records and Information Privacy Act 2002
- Section 27B of the NSW Privacy and Personal Information Protection Act 1998 No. 133
- Australian Research Data Commons (ARDC)
- Macquarie University’s Release of Student Information Policy and Guidelines
Contact us
The Ethics Secretariat administers the Maqcuarie University Human Research Ethics Committees (HRECs) and the Subcommittees.