Now working toward incorporating the core Australian codes

Research ethics, built into your proposal

From hypothesis to HREC-ready, reetre surfaces compliance obligations, integrity gaps, and regulatory requirements to help researchers and review committees to address proposals

National Statement on Ethical Conduct in Human Research (NS2023), Australia

An ethos that guides the approach taken by those engaged in human research.

NHMRC Research Integrity and Misconduct Policy, Australia

How to deal with things like suspected research misconduct and fraud.

Australian Code for the Responsible Conduct of Research, 2018

A framework for responsible research conduct that provides a foundation for high-quality research, credibility and community trust in the research endeavour.

Australian code for the care and use of animals for scientific purposes, 2013

Guidance for investigators, institutions, animals ethics committees, animal carers and all those involved in the care and use of animals for scientific purposes.

Global Reporting Standard for AI Disclosure in Research - in development

The Vancouver Standard aims to harmonise AI disclosure practices in research.

Sex inclusive research framework

An evaluation framework to assess whether an in vivo research proposal follows the sex inclusive research philosophy.

DFAT Ethical Research and Evaluation, 2021

Aligns and reinforces existing policies related to program management, conduct and risk management and safeguarding policies.

Cotton Research and Development Corporation

Facilitate the efficient and effective development and adoption of RD&E results to achieve maximum benefits to the cotton industry.

Animal Research: Reporting of In Vivo Experiments

Advice on experimental design, minimisation of bias, sample size and statistical analyses, helping the design of rigorous and reliable in vivo experiments.

AS/NZS 2243.3:2022 Microbiological Safety and Containment

Biosafety requirements needed to manage risks associated with handling biological agents and materials.

Research for Development Impact Network

Promote and support improved development practice in the areas of research and evaluation, to raise awareness, and to assist in the identification of ethical issues so that well-considered decisions can be made and justified.

Accelerated clinical trials

Protect research participants and to ensure the quality and trustworthiness of scientific advancements.

AIATSIS Code of Ethics for Aboriginal and Torres Strait Islander Research, 2020

Research with and about Aboriginal and Torres Strait Islander peoples follows a process of meaningful engagement and reciprocity between the researcher and the individuals and/or communities involved in the research.

Declaration of Helsinki

Respect for and protection of all research participants, including both patients and healthy volunteers.

National Statement on Ethical Conduct in Human Research (NS2023), Australia

An ethos that guides the approach taken by those engaged in human research.

NHMRC Research Integrity and Misconduct Policy, Australia

How to deal with things like suspected research misconduct and fraud.

Australian Code for the Responsible Conduct of Research, 2018

A framework for responsible research conduct that provides a foundation for high-quality research, credibility and community trust in the research endeavour.

Australian code for the care and use of animals for scientific purposes, 2013

Guidance for investigators, institutions, animals ethics committees, animal carers and all those involved in the care and use of animals for scientific purposes.

Global Reporting Standard for AI Disclosure in Research - in development

The Vancouver Standard aims to harmonise AI disclosure practices in research.

Sex inclusive research framework

An evaluation framework to assess whether an in vivo research proposal follows the sex inclusive research philosophy.

DFAT Ethical Research and Evaluation, 2021

Aligns and reinforces existing policies related to program management, conduct and risk management and safeguarding policies.

Cotton Research and Development Corporation

Facilitate the efficient and effective development and adoption of RD&E results to achieve maximum benefits to the cotton industry.

Animal Research: Reporting of In Vivo Experiments

Advice on experimental design, minimisation of bias, sample size and statistical analyses, helping the design of rigorous and reliable in vivo experiments.

AS/NZS 2243.3:2022 Microbiological Safety and Containment

Biosafety requirements needed to manage risks associated with handling biological agents and materials.

Research for Development Impact Network

Promote and support improved development practice in the areas of research and evaluation, to raise awareness, and to assist in the identification of ethical issues so that well-considered decisions can be made and justified.

Accelerated clinical trials

Protect research participants and to ensure the quality and trustworthiness of scientific advancements.

AIATSIS Code of Ethics for Aboriginal and Torres Strait Islander Research, 2020

Research with and about Aboriginal and Torres Strait Islander peoples follows a process of meaningful engagement and reciprocity between the researcher and the individuals and/or communities involved in the research.

Declaration of Helsinki

Respect for and protection of all research participants, including both patients and healthy volunteers.

National Statement on Ethical Conduct in Human Research (NS2023), Australia

An ethos that guides the approach taken by those engaged in human research.

NHMRC Research Integrity and Misconduct Policy, Australia

How to deal with things like suspected research misconduct and fraud.

Australian Code for the Responsible Conduct of Research, 2018

A framework for responsible research conduct that provides a foundation for high-quality research, credibility and community trust in the research endeavour.

Australian code for the care and use of animals for scientific purposes, 2013

Guidance for investigators, institutions, animals ethics committees, animal carers and all those involved in the care and use of animals for scientific purposes.

Global Reporting Standard for AI Disclosure in Research - in development

The Vancouver Standard aims to harmonise AI disclosure practices in research.

Sex inclusive research framework

An evaluation framework to assess whether an in vivo research proposal follows the sex inclusive research philosophy.

DFAT Ethical Research and Evaluation, 2021

Aligns and reinforces existing policies related to program management, conduct and risk management and safeguarding policies.

Cotton Research and Development Corporation

Facilitate the efficient and effective development and adoption of RD&E results to achieve maximum benefits to the cotton industry.

Animal Research: Reporting of In Vivo Experiments

Advice on experimental design, minimisation of bias, sample size and statistical analyses, helping the design of rigorous and reliable in vivo experiments.

AS/NZS 2243.3:2022 Microbiological Safety and Containment

Biosafety requirements needed to manage risks associated with handling biological agents and materials.

Research for Development Impact Network

Promote and support improved development practice in the areas of research and evaluation, to raise awareness, and to assist in the identification of ethical issues so that well-considered decisions can be made and justified.

Accelerated clinical trials

Protect research participants and to ensure the quality and trustworthiness of scientific advancements.

AIATSIS Code of Ethics for Aboriginal and Torres Strait Islander Research, 2020

Research with and about Aboriginal and Torres Strait Islander peoples follows a process of meaningful engagement and reciprocity between the researcher and the individuals and/or communities involved in the research.

Declaration of Helsinki

Respect for and protection of all research participants, including both patients and healthy volunteers.

How it works

Compliance embedded at every stage of research design

01

Describe your hypothesis

Your research question, methodology, and participant context, along with your regional, institutional and contractual engagements establish the framework applied for research review.

02

Generate a compliance map

The platform surfaces elements of guidelines and requirements under applicable guidelines, codes, policies, contracts, and community expectations.

03

Build your proposal

Assess insights and develop research proposals or reviews with feedback, case studies and best practices. Iterate with AI embedded tools to help build policy, legal, social and scientific integrity considerations.

Live compliance map

Cognitive load in remote surgery training

3 / 6 passed pre-review

Informed consent framework

Limited disclosure for active concealment proposed on the basis that the program involves no increased risk to the participant, there is no reason to think the participant would not consent and disclosure will be made after the program.

Responsive

Data governance plan

Interviews conducted by virtual meeting require a data management plan that addresses recordings made using those applications

Gap

Participant eligibility criteria

Participant criteria are representative of the affected population

Responsive

Cultural considerations

Research in a small community into attitudes to sub-populations may have effects on social cohesion or community dynamics

Review

Research merit

Relies on external peer review

Responsive

Conflict of interest disclosure

Funding sources may require bias consideration and information barriers during the research design process.

Review

Compliance maps update in real-time as you develop your proposal.

Public principles

Requirements of public codes, charters or regulations.

Private policies

Cross-check against private institutional or lab policies or contracted partner or funding commitments.

Audit trail

Every decision logged and triggered where research is adapted to new information.

Ethics narrative

AI assisted pre-review screening, preliminary analysis, consistency checking, and decision support to complement human judgement in research oversight and management.

resource constraints

Committees are widely understaffed, undertrained, and underfunded, especially at smaller institutions

uncertainty

Inconsistent or ambiguous interpretation of applicable regulations, and inefficiencies in review

cross-disciplinary value assessments

Ethics review is a multidimensional task that should be considered a collaborative effort

Framework

Every rule. Any source. Adaptable to your research.

Source-neutral topics that may apply across any instrument of research governance and compliance. Each framework, whether regulatory, institutional, or contractual expresses its own nuance within the same structure, and is applied or not based on a research proposal, participant characteristics, or institutional or funding context.

Filter by source
01
NSARCUKRI

Research merit and integrity

Whether the research proposes a contribution to the knowledge base, is designed with integrity and alignment with its objectives, and is conducted by qualified people.

02
NSGDPRICH

Risk, benefit and proportionality

Whether the likely program and outcomes justify any harms and fairly distribute any benefits to participants and wider society.

03
NSGDPRUKRIICH

Consent and autonomy

Informed choice, capacity, voluntariness with adequate disclosures and access to support off-ramps.

04
NSARC

Recruitment and equitable selection

Fair participant selection, equitable burden distribution, and protection from exploitation.

05
NSICHTGA

Participant and social welfare

Ongoing obligations during research and safety, privacy, adverse events, protocol deviations, debriefing.

06
NSGDPRPAARC

Data governance and privacy

Collection, storage, access, re-use in future projects, deletion and compliance.

07
NSARCUKRICOPE

Dissemination and results

Communication to participants, publication rights, and the obligation to report outcomes.

08
NSUKRIICH

Specific participant populations

Additional protections for participants whose circumstances limit free consent, heighten exposure to harm or vulnerability.

09
NSARCUKRI

Governance and accountability

Institutional oversight, ethics or expert review, conflicts of interest, and complaint pathways from hypothesis to reporting.

Governance tracks— additional obligations activated by research type
Human participants
HRECBaseline for all human research.
Children and youth
HRECAssent, guardian consent, child-safe.
Animal research
AEC3Rs, species protocols, endpoints, animal economics.
Biological specimens
IBCContainment levels, GMO, OGTR.
Dual use / military
Research officeDSGL, export controls, DFAT.
Hazardous chemicals
CSCWHS, Schedule 8/9, radiation.
Coming next
ARC & NHMRC funding integrityFunding guidelinesDFAT foreign interference controlsIP & commercialisation obligationsInstitutional biosafety frameworks
Ethics review is not a gate at the end of research design. It is the architecture of trustworthy research from the first question.
National Statement on Ethical Conduct in Human Research — NHMRC
Deep dives

Ethics in practice

Case studies exploring how research ethics obligations apply in real research contexts.

Guthrie cards

How newborn screening programs navigate consent, data retention, and the ethics of population-level health data collection.

Animals in research

The 3Rs framework, institutional oversight, and balancing scientific necessity with ethical responsibility to non-human subjects.

Researchers who push boundaries

He Jiankui went to prison for his controversial gene-editing research and practices. He's back in the lab and optimistic about advancing science. His case shows how those around his work navigated the ethical challenges.

Research interviews over video calls

Data management plans for remote research recruitment and study interviews should address privacy, consent, and data security.

The perception of corruption

Some populations are underrepresented in research. The ethical concerns with conducting studies in developing countries which would not be approved in developed countries is one consideration. The fear of being perceived as corrupt for conducting research in these regions is another.

Guthrie cards

How newborn screening programs navigate consent, data retention, and the ethics of population-level health data collection.