4.1 Informed Consent

• – Participation must be voluntary, with clear and plain-language explanations provided.
• – Informed consent must be documented prior to data collection.
• – Special care must be taken when involving children or vulnerable persons.

4.2 Privacy and Confidentiality

• – Personal data must be protected in accordance with the Privacy Act 1988.
• – Information will be de-identified unless explicit participant consent is obtained for identification.
• – Data must not be disclosed to third parties unless legally required.

4.3 Data Collection Standards

• – Research must not involve deception, coercion, or concealment of purpose.
• – Participants will not be misled about the intent or sponsor of the research.
• – Sensitive questions will only be asked when essential and treated with respect.

4.4 Professional Integrity

• – Projects must be methodologically sound, honest, and unbiased.
• – The distinction between factual findings and interpretations must be clear.
• – Conflicts of interest must be declared and managed.

4.5 Quality and Accuracy

• – All reports must reflect accurate, unaltered results.
• – Data storage must be secure and compliant with regulatory retention policies.
• – Findings must not be used to mislead stakeholders or the public.

4.6 Participant Protection

• – Every reasonable effort must be made to avoid harm, distress, or discomfort.
• – Participants must be given the option to withdraw at any stage.
• – Support resources will be made available where sensitive topics are involved.