Learn NDIS participants’ rights and responsibilities and how providers can stay compliant, build trust, and deliver person-centred care with confidence.

The National Disability Insurance Scheme (NDIS) empowers Australians with disability to have greater choice, control, and independence over the supports they receive. But with that empowerment comes an important framework of rights and responsibilities - not just for participants, but also for the providers who deliver services under the scheme.
For providers, understanding these principles isn’t just about compliance, it’s about building trust, delivering ethical services, and creating better outcomes for participants. Let’s explore what every provider should know.
The National Disability Insurance Scheme (NDIS) is grounded in the principles of choice and control, empowering participants to have a say in the services and supports they receive. This approach places individuals at the heart of decision-making, allowing them to choose the care they need and how it is delivered.
However, this empowerment also brings with it an important balance of responsibility. Participants are responsible for using their NDIS funding wisely, ensuring that their choices align with their plan goals, and not exceeding the limits of their funding.
For providers, understanding these principles is more than just about legal compliance - it’s about building a strong, ethical foundation for care. Providers who respect and uphold the rights of participants create transparent, respectful, and safe environments where participants feel valued and supported. This kind of environment fosters trust, collaboration, and satisfaction, which are essential for both the participants and the providers.
When providers understand and uphold these principles, they create transparent, respectful, and safe service environments. It also helps them stay compliant with the NDIS Code of Conduct and NDIS Practice Standards, reducing the risk of audit issues or complaints.

According to the National Disability Insurance Agency (NDIA), every NDIS participant has a set of clear rights designed to protect their dignity, independence, and choice.
As an NDIS provider, it’s essential to understand these rights and ensure your practices - from service delivery to communication - fully reflect them.
Participants have the right to:
To help providers put these principles into practice, here’s a quick overview of what each right means - and how providers should respond:
For providers, these rights shouldn’t just sit in policy documents - they must come alive in service agreements, communication, and everyday practice. Respecting participant rights isn’t optional; it’s the foundation of ethical, transparent, and compliant NDIS service delivery.
Just as participants have rights, they also have responsibilities that help ensure the NDIS operates fairly, efficiently, and with integrity.
Understanding these responsibilities is crucial not only for participants but also for providers, who play an important role in guiding and supporting participants to meet them.
Participants are responsible for:
For providers, having a clear understanding of these responsibilities helps maintain transparency and accountability. It also ensures services are appropriately billed and aligned with what’s considered “reasonable and necessary” under NDIS guidelines - protecting both the participant and the provider.
To help clarify how these responsibilities translate into daily practice, here’s an overview:
By understanding these shared responsibilities, providers can create a more transparent, ethical, and goal-driven care environment - where participants are empowered to take ownership of their supports, and providers remain compliant and trusted partners in their journey.
Every day, NDIS providers play a critical role in ensuring participants’ rights are respected and responsibilities are upheld. Translating principles into concrete actions helps build trust and promotes better outcomes for participants.
Here are some practical steps:
By consistently applying these steps, providers can create a safe, transparent, and participant-focused environment that upholds rights, strengthens trust, and ensures high-quality care for everyone involved.
Even the most well-meaning providers can sometimes unintentionally make errors that affect participant rights or responsibilities. Being aware of common pitfalls helps providers stay compliant and deliver ethical, high-quality care.
Common risks include:
How to avoid these issues:
By actively managing these risks, providers not only protect themselves but also safeguard participants’ rights, build trust, and ensure a higher standard of care.
At imploy, we understand the challenges of running a compliant and participant-focused NDIS business. That’s why we’ve developed a wide range of resources, templates, and guides to help providers stay on top of their obligations.
Explore tools such as:
With imploy, providers can simplify compliance and focus on what matters most - delivering high-quality, person-centred care.
Understanding NDIS participants’ rights and responsibilities is at the heart of good practice.
When providers respect participant rights and support participants in meeting their responsibilities, they create an environment built on trust, empowerment, and compliance.
By embedding these principles into every aspect of your operations - from service agreements to staff training - you’re not just following the rules; you’re helping participants live more independent and fulfilling lives.
Stay compliant, confident, and participant-focused - explore imploy’s NDIS compliance resources today.
1. Can a participant change providers if they’re unhappy?
Yes. Participants have the right to choose who delivers their supports and can change providers at any time.
2. Why is it important for NDIS providers to understand participants’ rights and responsibilities?
Understanding these principles helps providers deliver services that are ethical, transparent, and compliant with the NDIS Code of Conduct. It also builds trust and ensures participants receive the support they deserve.
3. What are the key rights of NDIS participants?
Participants have the right to choose their providers, refuse services, be free from pressure, ask about conflicts of interest, receive fair pricing, and control their personal information.
4: What should providers do if a conflict of interest arises?
Disclose it immediately, provide options, and document how the participant made their decision.
5. How can providers help participants meet their responsibilities?
By explaining plan limits, providing clear invoices, maintaining open communication, and regularly reviewing goals and progress to ensure supports remain aligned with their needs.