New ZealandPatient rights · HDC Code
The Code of Rights: What Each of the 10 HDC Rights Asks of NZ Health Practitioners
Every HDC complaint about your care is measured against the same ten rights. This guide reads the Code from the provider's side of the desk: what each right and subclause requires in day-to-day practice, how the clause 3 defence works, the breach patterns that recur in published HDC opinions, and what good practice looks like.
Reviewed October 2026 against the Code of Rights Regulations 1996, the Health and Disability Commissioner Act 1994, the Protection of Personal and Property Rights Act 1988, and Health and Disability Commissioner decisions, review documents and the 2024/25 annual report
Short answer: The Code of Rights gives every health and disability consumer in New Zealand ten legal rights, and places the matching duties on you as a provider: respect and privacy, freedom from discrimination and exploitation, dignity, a proper standard of care, effective communication, full information, informed choice and consent, support persons, protection in teaching and research, and a fair complaints process. HDC decides complaints by asking whether you met those duties. You are not in breach if you took reasonable actions in the circumstances, but under clause 3 it is up to you to show that.
Key takeaways
- The Code binds every "health care provider", which the HDC Act defines to include any health practitioner and anyone else who offers health services to the public, whether or not they charge.
- Right 4 (standard of care) covers the issues HDC receives most complaints about. In consent cases, a Right 6 breach about a procedure usually brings a Right 7(1) breach with it.
- Clause 3 is the only general defence: reasonable actions in the circumstances, including the consumer's clinical situation and your resource constraints. The onus sits on you, not the complainant.
- Consumers are presumed competent. Where they are not and no one is legally entitled to consent for them, Right 7(4) sets three conditions you must meet before providing services.
- HDC finds systems and organisations in breach more often than individuals, but an individual practitioner can still be found in breach alongside, or instead of, their employer.
- HDC recommended changes to the Act and Code in December 2024. As at October 2026 the Code wording in force is still the version as at 6 November 2021.
Why the Code is every practitioner's legal floor
The Code of Health and Disability Services Consumers' Rights is a regulation made under the Health and Disability Commissioner Act 1994. It has applied since 1 July 1996, and it is the yardstick for every complaint the Health and Disability Commissioner (HDC) handles. Our fitness to practise overview explains the route a complaint takes from HDC to your responsible authority and beyond. This guide deals with the content: what you are actually being measured against.
Three features make the Code different from the professional codes you sign up to on registration.
- It covers everyone who provides care, not just registered practitioners. The HDC Act defines a health care provider to include any health practitioner, ambulance services, people in charge of certified hospital and rest home services, and "any other person" who provides health services to the public or a section of it, whether or not they charge. A healthcare assistant, a practice, a district of Health New Zealand and a private clinic company are all providers.
- It is written as consumer rights with provider duties. Clause 1 says consumers have the rights, providers have the duties, and providers must take action to inform consumers of their rights and enable them to exercise them. Putting the Code poster on the wall is the minimum, not the whole duty.
- It sits above your professional code, not instead of it. Right 4(2) requires services that comply with legal, professional, ethical and other relevant standards, so a breach of your Council's code of conduct can become a Code of Rights breach too. Our comparison of NZ health practitioner codes of conduct shows what those professional standards contain.
Health and Disability Commissioner annual report 2024/25 (year to 30 June 2025). HDC also closed 4,406 complaints and made 809 recommendations, with 91% of those reviewed complied with.
Most complaints never reach a breach finding. HDC says around 68% of the complaints it closed in 2024/25 went through early resolution pathways. But the opinions it does publish show, in detail, how each right is interpreted, and those are the patterns this guide draws on.
How the Code is built: clauses 1 to 6
The Code is short. The ten rights sit inside clause 2, framed by clauses that decide who holds the rights, how compliance is judged and how the Code fits with other law. Practitioners tend to know the rights and skip the frame, yet the frame is where many HDC findings are won or lost.
| Clause | What it says | Why it matters to you |
|---|---|---|
| 1 | Consumers have rights; providers have duties, including a duty to inform consumers of their rights and enable them to exercise them | You must actively help people use their rights, not just avoid infringing them |
| 2 | The ten rights of consumers and duties of providers | The standard HDC applies to your care |
| 3 | No breach if you took reasonable actions in the circumstances; onus on the provider | Your only general defence, and it depends on your evidence |
| 4 | Definitions, including consumer, choice, exploitation and advance directive | Extends some rights to the person consenting on a consumer's behalf |
| 5 and 5A | The Code does not require you to break another law; 5A sets out how the Code works with the End of Life Choice Act 2019 | Where a statute authorises or requires an action, the Code does not override it |
| 6 | Rights that exist elsewhere are not lost because the Code leaves them out or covers them only in part | The Code is a floor; common law and other statutes still apply |
Clause 3: the reasonable actions defence
Clause 3 is the provision every practitioner should know by heart. It says a provider is not in breach of the Code if it has taken reasonable actions in the circumstances to give effect to the rights and comply with the duties. Two further subclauses do the heavy lifting:
- The onus is on you. Clause 3(2) puts the burden of proving reasonable actions on the provider. The consumer does not have to prove you acted unreasonably.
- "The circumstances" are broad. Clause 3(3) says they mean all the relevant circumstances, including the consumer's clinical circumstances and the provider's resource constraints.
In practice this means a breach finding often turns on what you can show, years after the event. HDC investigations commonly run for a long time, and your memory of a ten-minute consultation will not carry the weight of a contemporaneous note. The defence is strongest when your record shows what you knew, what you considered, what you told the consumer and why you chose the path you did.
What clause 3 can cover
An emergency where there was genuinely no time for a full consent discussion; a rural service without on-site specialist backup; an unexpected complication managed reasonably; a resource limit outside your control, provided you did what you reasonably could within it, such as escalating or telling the consumer about the limit.
What it rarely rescues
Ignoring a stated refusal; skipping a check the consumer was told would happen; failing to act on an abnormal result; not documenting a competence assessment; "we were busy" offered without evidence of what you did to manage the risk.
The decisions discussed below show the line. In a 2026 opinion about a planned Caesarean, the Commissioner accepted that the obstetrician believed she was acting in the woman's best interests and that a Caesarean was probably the clinically preferred option, but still found a breach because the situation was not an emergency and there was time to pause and tell the woman that the promised check on her baby's position had not been done. Good intentions and a defensible clinical plan did not prevent a breach finding.
HDC's 2024 review rejected calls for a separate exemption from the Code during public health emergencies, saying such emergencies should not override people's rights as a matter of course and that clause 3 already allows them to be taken into account.
Clause 4 definitions that change how the rights apply
Several definitions widen or sharpen the rights in ways that catch practitioners out.
| Term | Definition in short | Practical effect |
|---|---|---|
| Consumer | A health or disability services consumer; for Rights 5, 6, 7(1), 7(7) to 7(10) and 10, it includes a person entitled to consent on the consumer's behalf | An attorney or welfare guardian with authority to consent is owed the consumer's communication, information, consent-related and complaint rights under those provisions |
| Choice | A decision to receive services, to refuse them, or to withdraw consent | Refusal and withdrawal are informed choices too, and need the same information |
| Exploitation | Includes abuse of a position of trust, breach of a fiduciary duty and undue influence | Right 2 reaches beyond sexual misconduct to financial dealings, gifts and pressure |
| Discrimination | Discrimination that is unlawful under Part 2 of the Human Rights Act 1993 | Right 2 imports the prohibited grounds in human rights law |
| Optimise the quality of life | Taking a holistic view of the consumer's needs to achieve the best possible outcome in the circumstances | Right 4(4) is about the whole person, not just the presenting problem |
| Advance directive | A written or oral directive by which a consumer makes a choice about a possible future procedure, intended to apply only when they are not competent | An oral directive can count; record any you are told about |
| Teaching | Includes the training of providers | Students and trainees involved in care bring Rights 6(1)(d) and 9 into play |
| Services | Health services, disability services, or both, including health care procedures | The Code covers assessment, advice and support, not just treatment |
The 10 rights at a glance
Before going right by right, here is the whole Code on one screen, framed as the duty each right places on you.
| Right | Your duty in one line | Where breaches tend to arise |
|---|---|---|
| 1. Respect | Treat people with respect, protect privacy, and take account of cultural, religious, social and ethnic needs, including those of Māori | Dismissive manner, privacy lapses, ignoring cultural needs |
| 2. Freedom from discrimination, coercion, harassment and exploitation | Never use your position for sexual, financial or other advantage, or pressure people | Boundary violations, undue influence, discriminatory treatment |
| 3. Dignity and independence | Deliver care in a way that respects dignity and supports independence | Personal cares, exposure, infantilising older or disabled people |
| 4. Appropriate standard | Reasonable care and skill; meet professional standards; meet needs; minimise harm; co-operate with other providers | Missed results, poor assessment, failed handovers, no one in charge |
| 5. Effective communication | Communicate in a form, language and manner the person understands, with an interpreter where needed and reasonably practicable | No interpreter, jargon, closed or rushed conversations |
| 6. Fully informed | Give the information a reasonable consumer in their circumstances would expect, including options, risks, results and honest answers | Results not passed on, risks and alternatives not discussed |
| 7. Informed choice and consent | Provide services only with informed consent, unless the law provides otherwise; presume competence; respect refusal | Going beyond what was consented to, poor capacity assessment |
| 8. Support | Allow support persons of the consumer's choice, unless safety or another consumer's rights would be compromised | Whānau excluded without good reason |
| 9. Teaching and research | Apply every right when people take part in teaching or research | Students present or examining without the consumer's agreement |
| 10. Complaints | Make complaining easy, and resolve complaints fairly, simply, speedily and efficiently | Defensive or slow responses, withholding information |
Rights 1 to 3: respect, exploitation and dignity
These three rights are short, but they reach into every encounter. They are often found alongside other breaches rather than alone, and they are the rights most closely tied to how the consumer felt they were treated.
Right 1: respect, privacy and cultural needs
Right 1 has three parts. Every consumer has the right to be treated with respect (1(1)), to have their privacy respected (1(2)), and to receive services that take into account the needs, values and beliefs of different cultural, religious, social and ethnic groups, including the needs, values and beliefs of Māori (1(3)).
- Respect is judged from conduct: how you speak to people, whether you listen, whether you belittle concerns. HDC's complaint data counted 138 complaints in 2024/25 where a disrespectful manner or attitude was the primary issue.
- Privacy in Right 1(2) overlaps with the Health Information Privacy Code but is wider than information. It also covers physical privacy: curtains, exposure, conversations overheard in shared rooms. For the information side, see our guide to the Health Information Privacy Code 2020 in clinical practice.
- Cultural needs under Right 1(3) are an explicit legal duty, not just a professional expectation. Asking about whānau involvement, karakia, language preference or tapu around the body, and acting on what you learn, is how you meet it. The professional requirements behind this are compared in our article on cultural safety CPD requirements.
Right 2: freedom from discrimination, coercion, harassment and exploitation
Right 2 protects consumers from discrimination, coercion, harassment, and sexual, financial or other exploitation. Read with the clause 4 definition, exploitation includes abuse of a position of trust, breach of a fiduciary duty and undue influence. That captures far more than sexual misconduct: accepting significant gifts, borrowing money, involving patients in your business, or pressing a decision on someone who depends on you.
- Facts
- A mental health nurse who had provided care to a prisoner left her role, moved overseas and later gave him her personal phone number. There were 47 recorded calls over about five months in 2020; eleven included sexually explicit comments, mainly from him, which she did not clearly rebuff.
- Finding
- Breach of Right 4(2), for initiating and engaging in personal, often intimate contact after the therapeutic relationship ended, and of Right 2, because the relationship was exploitative.
- Reasoning
- The power imbalance did not end with the professional relationship. He remained in prison and in mental health care, and she held sensitive information about him. The Nursing Council's guidance sets no arbitrary time limit on relationships with former patients.
- Lesson
- Ending the therapeutic relationship does not end your Right 2 duty. Vulnerability and the information you hold are what matter.
If boundaries are a live issue for you or your team, the professional boundaries course works through these situations in more depth.
Right 3: dignity and independence
Right 3 is a single sentence: services must be provided in a manner that respects the dignity and independence of the individual. It is most often engaged in aged residential care, disability support and inpatient settings, where personal cares, continence, mobility and choice about daily routines are part of the service. Practical tests: would the person choose to be left like this? Are you doing for them what they could do for themselves with time and support? Have you asked, or decided for them?
Right 4: services of an appropriate standard
Right 4 is the clinical heart of the Code and the right most practitioners picture when they think of an HDC complaint. It has five subclauses, and each one is assessed on its own.
| Subclause | Requirement | How HDC typically tests it |
|---|---|---|
| 4(1) | Services provided with reasonable care and skill | Independent advice from a peer in the same field on whether the care departed from accepted practice, and how far |
| 4(2) | Services that comply with legal, professional, ethical and other relevant standards | Comparison with your Council's code and standards, national guidelines and your organisation's policies |
| 4(3) | Services provided in a manner consistent with the consumer's needs | Whether care was tailored, for example to disability, age, language or frailty |
| 4(4) | Services that minimise potential harm to, and optimise the quality of life of, the consumer | Whether foreseeable risks were managed and the whole person considered |
| 4(5) | Co-operation among providers to ensure quality and continuity of services | Handovers, referrals, results management and whether anyone owned the care pathway |
Right 4(1): reasonable care and skill
The test is what a reasonable practitioner in your field would have done, not what a perfect one would have done with hindsight. HDC usually obtains independent clinical advice from a practitioner in the same discipline, who is asked whether your care was consistent with accepted practice and, if not, how serious the departure was. Missed or delayed follow-up of abnormal results is a recurring Right 4(1) pattern.
- Facts
- Routine bloods in 2017 showed a raised PSA. The GP did not tell the man or refer him. Over three years of further visits for ongoing symptoms the result was never raised. A repeat PSA in 2020 led to a diagnosis of metastatic prostate cancer.
- Finding
- Right 4(1), because the GP did not take appropriate action on the abnormal result and his management was not consistent with Ministry of Health guidance. Right 6(1), because he did not tell the man about the result within a reasonable time.
- Outcome
- Apology, referral to the Medical Council to consider a competence review, learning on sharing test results, and an audit of practice policies.
- Lesson
- One missed result can breach two rights at once: the clinical response (Right 4) and the duty to tell (Right 6).
Results management is a good place to test your own systems. Our list of medical audit ideas for NZ GPs includes ready-made audits on overdue results and referral follow-through.
Right 4(2): professional and legal standards
Right 4(2) is the bridge between the Code and your profession's own rules. Your Council's code of conduct, its standards and statements, clinical guidelines, legislation and your employer's policies are all "relevant standards". Working outside your authorised scope can also be a Right 4(2) issue; our guide to scopes of practice under the HPCA Act explains where those limits come from.
Right 4(3) and 4(4): fitting care to the person
These subclauses ask whether care was right for this consumer, not just technically adequate. A discharge plan that assumes a frail person can manage stairs and medicines alone, or a pain plan that ignores someone's known history, can fall short here even when each individual step looks reasonable.
Right 4(5): co-operation and continuity
Right 4(5) is where organisations are most often found in breach, because continuity depends on systems: who owns a referral, who follows up a result, how a handover is done. It is also the subclause most relevant to shared care across primary and secondary services.
- Facts
- A woman with a small, low-grade breast cancer was managed by a breast service in which no single clinician held overall responsibility. She first met her operating surgeon on the morning of surgery, when newly disclosed family history led him to raise the option of delaying surgery; she chose to proceed. She later chose bilateral mastectomy with implant reconstruction, which had complications.
- Finding
- The district breached Right 4(5): the system did not assign clear responsibility for her care. The surgeon breached Right 6(1) by not adequately counselling her on the benefits, risks and alternatives of prophylactic mastectomy, and therefore Right 7(1).
- Note
- The Commissioner was not critical of the surgical skill and care. Raising alternatives on the morning of surgery was inappropriate, but the Commissioner did not consider that wholly the surgeon's fault, given the system he was working in.
- Lesson
- Individual and organisational findings can sit side by side, each assessed against a different subclause.
Right 5: effective communication
Right 5 has two subclauses. Right 5(1) gives every consumer the right to effective communication in a form, language and manner that enables them to understand the information provided; where necessary and reasonably practicable, this includes the right to a competent interpreter. Right 5(2) gives every consumer the right to an environment that enables both consumer and provider to communicate openly, honestly and effectively.
Communication is one of the most common things complaints are about. In 2024/25 failure to communicate effectively with the consumer was the primary issue in 165 complaints to HDC, fifth on its list.
Health and Disability Commissioner annual report 2024/25, primary complaint issues table. Each complaint is counted once, under its primary issue.
Communication failures also sit underneath many of the treatment and diagnosis complaints above: a worsening symptom not reported because the consumer did not know it mattered, or a plan misunderstood at discharge. What Right 5 asks of you in practice:
- Interpreters. "Where necessary and reasonably practicable" means you need a reason, recorded, for not using a competent interpreter when the consumer's English is limited. Using a child or a distressed relative to interpret serious news rarely meets the standard of a competent interpreter.
- Form and manner. Plain language, written or visual information where it helps, extra time for people with cognitive impairment, sensory loss or a learning disability, and checking understanding with teach-back rather than asking "Any questions?".
- An open environment. Right 5(2) is about conditions as well as words: privacy for difficult conversations, permission to ask, and a culture where people are not made to feel a nuisance. It is also the right that underpins open disclosure when something goes wrong; the open disclosure training covers how to have those conversations.
Right 6: the right to be fully informed
Right 6 sets the information standard, and it is consumer-centred. Right 6(1) entitles every consumer to the information that a reasonable consumer, in that consumer's circumstances, would expect to receive. The question is not what a reasonable doctor or nurse would usually say, but what a reasonable person in this patient's position would want to know.
Right 6(1) lists what that includes:
- An explanation of their condition (6(1)(a))
What is wrong, or what you think may be wrong, in terms they can follow.
- The options available (6(1)(b))
Including an assessment of the expected risks, side effects, benefits and costs of each option. Doing nothing, waiting and referral elsewhere are options too.
- Timeframes (6(1)(c))
Advice of the estimated time within which services will be provided, such as waiting times for a procedure or a specialist appointment.
- Teaching or research (6(1)(d))
Notification of any proposed participation in teaching or research, including whether the research requires and has received ethical approval.
- Anything else required by standards (6(1)(e))
Information that legal, professional, ethical and other relevant standards require you to give.
- Results (6(1)(f) and (g))
The results of tests and of procedures. A result you have seen but not passed on is a classic Right 6 breach.
Three further subclauses complete the right:
- Right 6(2): before making a choice or giving consent, every consumer has the right to the information a reasonable consumer in their circumstances needs to make an informed choice or give informed consent. This is the bridge to Right 7.
- Right 6(3): every consumer has the right to honest and accurate answers to questions about services, including your identity and qualifications, your recommendation, how to get an opinion from another provider, and the results of research.
- Right 6(4): on request, a written summary of the information provided.
In published opinions about procedures, HDC very often finds a breach of Right 6(1) or 6(2) first, then a breach of Right 7(1) "as a consequence": because the consumer did not have the information they needed, they could not give informed consent. If your information is deficient, the consent falls with it.
Good practice under Right 6 is less about longer consent forms and more about the conversation: individualised risks rather than generic lists, alternatives including no treatment, your own recommendation and why, and a note recording what was discussed. Where the consumer asks about your experience with a procedure, Right 6(3) requires an honest answer.
Right 7: informed choice and informed consent
Right 7 is the longest right in the Code, with ten subclauses. Its opening sentence sets the default: services may be provided to a consumer only if that consumer makes an informed choice and gives informed consent, except where any enactment, the common law, or any other provision of the Code provides otherwise.
Competence: the presumption and diminished competence
Right 7(2) says every consumer must be presumed competent to make an informed choice and give informed consent, unless there are reasonable grounds for believing the consumer is not competent. Right 7(3) adds that a consumer with diminished competence keeps the right to make informed choices and give informed consent to the extent appropriate to their level of competence.
Two things follow. First, you need reasonable grounds, not a hunch or a diagnosis label, to depart from the presumption. Second, competence is decision-specific: a person may be able to consent to a blood test but not to complex surgery, or to everyday care but not to a major financial or residential decision.
- Facts
- A 16-year-old with fetal alcohol spectrum disorder and ADHD, assessed by a specialist as having the mental capacity of a child, asked a nurse to remove her contraceptive implant. Her grandmother, a court-appointed guardian, phoned to say she lacked capacity for the decision and asked the nurse to wait for specialist information. After talking with her and consulting senior staff, the nurse assessed her as competent and removed the implant.
- Finding
- The organisation breached the Code by failing to provide services with reasonable care and skill. It lacked adequate protocols for assessing capacity in young people with intellectual impairment. The nurse was criticised for not deferring her decision until the guardian's concerns were clarified.
- Reasoning
- Competence is presumed, but where there are reasonable grounds to doubt it the provider must carry out an adequate assessment. The red flags should have prompted a delay while information was gathered.
- Lesson
- When someone with knowledge of the person raises a capacity concern, pause, gather information and document your assessment and reasons.
Right 7(4): when the consumer is not competent
Where a consumer is not competent to make an informed choice and give informed consent, and no person entitled to consent on their behalf is available, Right 7(4) allows you to provide services only if all of these conditions are met:
- Best interests
It is in the consumer's best interests.
- Reasonable steps to find out their views
You have taken reasonable steps to ascertain the views of the consumer.
- One of two further tests
Either, if their views have been ascertained and you have reasonable grounds to believe the service is consistent with the informed choice they would make if competent, you proceed on that basis; or, if their views have not been ascertained, you take into account the views of other suitable persons who are interested in the consumer's welfare and available to advise you.
Note the order. Right 7(4) applies only when no one entitled to consent is available. Under the Protection of Personal and Property Rights Act 1988, that person is usually a court-appointed welfare guardian or an attorney under an enduring power of attorney for personal care and welfare. An attorney can act only if the person is mentally incapable, and for a significant matter, such as a major medical procedure, only once a relevant health practitioner has certified, or the court has determined, that the person is mentally incapable. Neither a welfare guardian nor an attorney can refuse consent to standard medical treatment intended to save the person's life or prevent serious damage to their health. Where one of them is available, clause 4 extends Rights 5, 6, 7(1), 7(7) to 7(10) and 10 to them. Whānau who hold no legal authority do not consent on the person's behalf, but under Right 7(4)(c)(ii) their views are exactly what you should seek and record where the person's own views cannot be ascertained. The legal framework for attorneys and welfare guardians is covered in the decision-making capacity and PPPR Act course.
Advance directives, writing and refusal
- Right 7(5): every consumer may use an advance directive in accordance with the common law. For assisted dying only, clause 5A says Rights 7(2) to 7(5) are overridden by the End of Life Choice Act 2019's own competence test.
- Right 7(6): where informed consent is required, it must be in writing if the consumer is to participate in research; the procedure is experimental; the consumer will be under general anaesthetic; or there is a significant risk of adverse effects on the consumer.
- Right 7(7): every consumer has the right to refuse services and to withdraw consent to services. A refusal you disagree with is still a valid choice if it is informed and the person is competent.
- Right 7(8): every consumer has the right to express a preference about who provides services and to have that preference met where practicable, such as a request for a female clinician for an intimate examination.
- Rights 7(9) and 7(10): consumers may decide about the return or disposal of body parts or bodily substances removed during a procedure. These may be stored, preserved or used only with informed consent, for ethics-committee-approved research, or for specified quality activities such as a professionally recognised quality assurance programme or an external audit or evaluation of services.
A signed form shows that a consent process happened. It does not prove the consumer received the information Right 6 requires. HDC looks at the discussion, so record the key risks, alternatives and questions in your notes as well.
Consent breaches in practice
Two recent opinions show the most common Right 7 failure: doing something different from what the consumer agreed to, without going back to them.
A stated refusal overridden
A woman told her team she wanted endometriosis lesions excised, not ablated, and her consent form recorded excision only. A surgeon who stepped in ablated a small lesion near the bowel without re-consenting her. Breach of Right 6(2) and Right 7(1). The Commissioner rejected arguments that this was only a preference and that express consent for individual techniques is not standard practice.
A promised check skipped
A planned Caesarean for a presumed breech baby went ahead without the ultrasound the consultant had requested to confirm position, and without telling the woman. The baby was head-down. Breach of Right 6(1) and Right 7(1): her consent was based on the position being checked first, and this was not an emergency.
In both cases the clinical skill was not the problem. The lesson is simple and practical: if circumstances change after consent is given, or a step the consumer relied on has not happened, stop and tell them before you proceed, unless there is a genuine emergency. Our audit ideas include a consent documentation audit if you want to test your own records.
Rights 8 and 9: support persons, teaching and research
Right 8: the right to support
Every consumer has the right to have one or more support persons of their choice present, except where safety may be compromised or another consumer's rights may be unreasonably infringed. The exceptions are narrow. Excluding whānau because it is inconvenient, because the room is small or because staff find a family member challenging is unlikely to meet them. Where you do limit support people, record the safety or rights reason and revisit it. HDC's 2024 review recommended strengthening this right, including allowing support people to be involved when they cannot be physically present, but that recommendation is not yet law.
Right 9: teaching and research
Right 9 says the rights in the Code extend to consumers taking part, or proposed to take part, in teaching or research. It works with two other provisions: Right 6(1)(d), which requires you to tell consumers about any proposed participation in teaching or research, and Right 7(6)(a), which requires written consent to research. Because "teaching" includes the training of providers, a student observing, examining or performing a procedure engages these rights. Ask the consumer in advance, make it easy to say no, and record the answer, especially for intimate examinations and anaesthetised patients.
Right 10: complaints
Right 10 gives consumers the right to complain about a provider in any form appropriate to them, to the provider, to anyone authorised to receive complaints, or to others such as an independent advocate or HDC. It then sets out how providers must handle complaints. The key duties and timeframes:
Facilitate the fair, simple, speedy and efficient resolution of complaints (10(3)), and keep complying with all the other rights while you do so (10(5)).
Acknowledge the complaint in writing, unless it has been resolved to the consumer's satisfaction in that time (10(6)(a)).
Decide whether you accept the complaint is justified, or, if more time is needed, decide how much; if that is more than 20 working days, tell the consumer how long and why (10(7)).
Update the consumer on progress (10(4)).
As soon as practicable, tell the consumer the reasons for the decision, any actions you propose and any appeal procedure (10(8)).
Right 10(6) requires every provider, unless an employee of a provider, to have a complaints procedure that also informs the consumer of internal and external complaint options, including advocates and HDC, documents the complaint and your actions, and gives the consumer all relevant information you hold. If you are employed, your employer's procedure applies, but the other duties in Right 10 still apply to you personally.
Right 10 can be breached on its own. In Director of Proceedings v Wilding International Ltd [2021] NZHRRT 45, a rest home operator that declined or ignored at least ten HDC requests for a resident's clinical notes was declared in breach of Right 10(3), which HDC's Director of Proceedings understood to be the first such finding. A defensive, slow or obstructive response can create a breach where the original care might not have.
This guide does not cover how to respond to an HDC letter step by step. If you are dealing with one, the responding to a complaint course and the process sections of our fitness to practise overview are the places to start.
How HDC decides whether the Code was breached
Knowing how breach opinions are built helps you understand what the Code asks of you on an ordinary day. Without going into the complaint process itself, these are the features that recur.
Individual and organisational providers
HDC assesses each provider involved separately: the individual practitioner, the practice or clinic, and the district or company that runs the service. Its 2024/25 annual report notes that systems and organisations are found in breach of the Code more often than individuals. Many published opinions find an organisation in breach for systemic failures while making only an adverse comment, not a breach finding, about an individual, or the reverse. In 20HDC01421, the surgeon was found in breach and Health New Zealand was not, though HDC commented adversely that its response focused on clinical judgement rather than the patient's right to refuse.
Employer liability under section 72
Section 72 of the HDC Act makes an employing authority responsible for its people. Anything done or omitted by an employee is treated as done or omitted by the employer as well as by the employee, whether or not the employer knew or approved. Acts of agents and members are treated the same way, unless they acted without the authority's express or implied authority. Under section 72(5), an employer has a defence if it proves it took such steps as were reasonably practicable to prevent the employee from doing the act or omission, or acts of that description.
For you as an employee, the point is that your employer's potential liability does not replace your own. HDC can find the individual in breach, the employer directly in breach for its systems, the employer vicariously liable for the employee, or any combination. HDC's 2024 review also asked the Ministry of Health to look at changing the wording of section 72, but no change has been made.
Outcomes of a breach finding
When HDC forms the opinion that a provider breached the Code, the HDC Act allows the Commissioner to report to the provider with recommendations, report to the provider's responsible authority or other bodies, and refer the provider to the Director of Proceedings, who decides whether to take proceedings. In the decisions in this guide, typical recommendations were a written apology, HDC's online learning modules, an audit of records or policies, and, for one GP, referral to the Medical Council to consider a competence review. In 2024/25 HDC referred 12 providers to the Director of Proceedings.
What happens next with your responsible authority depends on your profession; see the MCNZ complaint process, the Nursing Council complaint process or the Professional Conduct Committee guide.
Across the decisions, providers fared better where contemporaneous notes showed the reasoning, where concerns from whānau were documented and acted on, where systems made one person clearly responsible, and where the provider had already made changes and apologised by the time HDC reported.
Is the Code changing? The 2024 review
The HDC Act requires regular reviews of the Act and Code. HDC's latest review ran from 2023, and it delivered its recommendations to the Minister of Health in December 2024. Here is what is verified as at October 2026.
Review scoped by HDC.
Public consultation; HDC received 259 submissions.
Recommendations delivered to the Minister of Health.
Recommendations report tabled in Parliament.
Code text in force remains the version as at 6 November 2021. We found no Government bill to implement the review's recommendations.
HDC concluded the Act and Code are generally working well and recommended mostly targeted changes. Those relevant to the rights in this guide include:
- adding tikanga to the cultural needs wording in Right 1(3);
- strengthening the right to support to make decisions, and allowing support people to take part when they cannot be physically present;
- a right to support to make a complaint, and more explicit protection against retaliation for people who complain;
- replacing "under general anaesthetic" in Right 7(6)(c) with wording about medication given to alter consciousness, awareness or recall for the procedure.
HDC recommended that Code changes be finalised once the policy direction for the Act is clear, alongside other reforms including the review of the Health Practitioners Competence Assurance Act. It is up to the Government whether to progress them. For the HPCA side of that reform, see our article on the HPCA Amendment Bill 2026. Until the Code is formally amended, HDC will keep assessing complaints against the current wording.
Practitioner checklist: the Code in your next clinic
Use this as a quick self-audit. Each item maps to the right it protects.
- I introduce myself and my role, and answer honestly if asked about my qualifications or experience (Right 6(3)).
- I ask about cultural, religious and whānau needs and act on the answers (Right 1(3), Right 8).
- Physical privacy and confidentiality are protected during examinations and conversations (Right 1(2)).
- I use a competent interpreter where needed, or record why it was not reasonably practicable (Right 5(1)).
- I check understanding with teach-back, not "Any questions?" (Right 5(1)).
- I explain options, including no treatment, with risks, benefits and costs relevant to this person (Right 6(1)(b), 6(2)).
- Every result I order has a named person responsible for acting on it and telling the consumer (Rights 4(1), 4(5), 6(1)(f)).
- I start from the presumption of competence, and document a decision-specific assessment where I have reasonable grounds to doubt it (Right 7(2), 7(3)).
- Where a person lacks competence, I find out who can legally consent, and if no one can, I meet and record all three Right 7(4) conditions.
- I get written consent for research, experimental procedures, general anaesthesia and significant-risk procedures (Right 7(6)).
- If anything changes after consent, I stop and re-consent unless it is a genuine emergency (Right 7(1)).
- Students and trainees are involved only with the consumer's agreement (Rights 6(1)(d), 9).
- I respond to complaints openly, on time and without defensiveness (Right 10).
- Relying on a signed form alone as proof of informed consent.
- Using family members, especially children, to interpret serious information.
- Personal, financial or intimate contact with a current or former patient where a power imbalance remains.
- Leaving whānau out of decisions for someone who lacks competence.
- Assuming someone else will follow up a result or referral.
Self-check: which right is engaged?
Try each scenario before opening the answer.
During a procedure you find a second abnormality and treat it while the patient is sedated. They agreed only to the first. It was not urgent. Which rights are at risk?
A man with mild dementia refuses a flu vaccine. His daughter, who has no legal authority, asks you to give it anyway. What does the Code say?
A patient with limited English is seen without an interpreter because the phone service had a 20-minute wait. Is that a breach?
Your practice has no system for tracking whether referred patients are seen. A patient's urgent referral is lost. Who could be in breach?
A former client offers you a share in their business, months after your care ended. Can Right 2 still apply?
A consumer complains in writing. Your practice manager is on leave and nobody replies for three weeks. Which subclauses are engaged?
Frequently asked questions
Does the Code of Rights apply to unregistered health workers?
Yes. The HDC Act defines a health care provider to include any health practitioner and any other person who provides health services to the public or a section of it, whether or not they charge. Healthcare assistants, support workers, unregistered therapists and the organisations that employ them are all covered.
Is the Code of Rights the same as my Council's code of conduct?
No. The Code of Rights is a regulation enforced by HDC and applies to all providers. Your responsible authority's code of conduct sets professional standards for your profession. They connect through Right 4(2), which requires care that complies with professional and ethical standards, so a serious breach of your professional code can also be a breach of the Code of Rights.
Which right is breached most often?
HDC's annual report does not publish breach counts by right. Its complaint data shows the most common primary issues are inadequate treatment, missed or delayed diagnosis and delay in treatment, which usually engage Right 4. Published opinions about procedures very often find breaches of Rights 6 and 7(1) together.
Can I be in breach if my employer's system caused the problem?
You can, but HDC assesses each provider separately. It often finds the organisation in breach for systemic failures, sometimes with only an adverse comment about the individual. Under section 72 of the HDC Act your employer can also be liable for your acts or omissions unless it shows it took reasonably practicable steps to prevent them. Clause 3 lets you show your own actions were reasonable given the resources you had.
Does a signed consent form protect me from a Right 7 breach?
Not on its own. Right 7(6) requires written consent in some situations, but the form is evidence that consent was obtained, not proof that the consumer received the information Right 6 requires. HDC looks at what was actually discussed, so your clinical notes on risks, alternatives and questions matter as much as the signature.
Who can consent for an adult who lacks capacity?
Only a person legally entitled to consent on their behalf, usually a court-appointed welfare guardian or an attorney under an enduring power of attorney for personal care and welfare who is able to act because the person is mentally incapable. Neither can refuse standard treatment intended to save life or prevent serious damage to health. If no such person is available, Right 7(4) allows you to proceed only where the service is in the person's best interests, you have taken reasonable steps to find out their views, and you have either acted consistently with those views or, if they cannot be found out, considered the views of suitable people interested in their welfare.
Has the Code of Rights been changed recently?
The last amendment to the Code text was on 6 November 2021, when clause 5A was added for the End of Life Choice Act 2019. HDC delivered recommendations for further changes to the Minister of Health in December 2024, but as at October 2026 those are proposals for the Government to decide on, not law.
Do I have to tell patients about the Code?
Clause 1 requires providers to take action to inform consumers of their rights and enable them to exercise them. Displaying HDC's Code information is common, but the duty also means telling people how to raise concerns and complain, and supporting them to do so, as Right 10 sets out.
Primary sources
16 official documents
- New Zealand Legislation: Health and Disability Commissioner (Code of Health and Disability Services Consumers' Rights) Regulations 1996
- New Zealand Legislation: Health and Disability Commissioner Act 1994
- New Zealand Legislation: Protection of Personal and Property Rights Act 1988
- Health and Disability Commissioner: Code of Health and Disability Services Consumers' Rights
- Health and Disability Commissioner: Annual Report 2024/25
- Health and Disability Commissioner: Annual report shows major lift in complaint resolution
- Health and Disability Commissioner: Review of the Act and Code 2024
- Health and Disability Commissioner: Review of the HDC Act and Code, Recommendations Report (December 2024)
- Health and Disability Commissioner: Review of the HDC Act and Code, Executive Summary (March 2025)
- Health and Disability Commissioner: Decision 20HDC01421
- Health and Disability Commissioner: Decision 25HDC00165
- Health and Disability Commissioner: Decision 20HDC00204
- Health and Disability Commissioner: Decision 19HDC00666
- Health and Disability Commissioner: Decision 20HDC01728
- Health and Disability Commissioner: Decision 21HDC00473 media release
- Health and Disability Commissioner: Director of Proceedings v Wilding International Ltd [2021] NZHRRT 45