Funding up to $5 million to help Australian digital and connected health SMEs accelerate commercialisation, build clinical evidence, attract investment and achieve market growth.
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What is ANDHealth+?
ANDHealth+ is a commercialisation acceleration program supporting innovative Australian digital and connected health SMEs with technologies that demonstrate potential for commercial and clinical impact.
Supported by the Australian Government through the Medical Research Future Fund (MRFF) Medical Research Commercialisation Initiative, the program combines non-dilutive project funding with specialist expertise, hands-on support and access to a global network of industry advisors, investors, clinicians, executives and corporate partners.
The program targets evidence-based technologies that have reached or substantially demonstrated proof of concept and have a clear focus on improving patient outcomes.
Up to five companies are selected in each intake through a competitive assessment process.
ANDHealth+ level of support
Funding Amount
- Minimum funding: No minimum funding amount per applicant is specified by ANDHealth.
- Maximum funding: Up to $5 million per SME across approved Stage 1, Stage 2 and any follow-on funding activities.
- Stage 1: Five SMEs in each intake share a funding pool of $1.5 million.
- Stage 2: Five SMEs in each intake share a funding pool of $7.5 million.
- Follow-on funding may be awarded competitively from unallocated Stage 1 and Stage 2 funding.
- Funding is non-dilutive, with no equity requirement or transfer of intellectual property to ANDHealth.
- Significant in-kind support, specialist expertise and hands-on resources are also provided.
- Funding is generally paid directly by ANDHealth to third-party suppliers on behalf of participating companies.
- In some circumstances, funds may be paid directly to participating companies for agreed expenditure, subject to verification.
- Funding is released in tranches based on achievement of agreed milestones and successful navigation of go/no-go points.
Co-contribution
- No specified co-contribution or matched-funding percentage is stated in the ANDHealth+ program information.
- Applicants must, however, have sufficient financial and operational resources to continue their normal business operations while participating.
- Applicants must demonstrate at least 6–12 months of operating runway, with evidence of at least 12 months preferred.
- ANDHealth+ funding is intended for direct approved project costs rather than normal operating expenses such as day-to-day salaries and business overheads.
- Administrative costs associated with completing project activities are subject to a 10% funding limit.
ANDHealth+ important dates
- Applications close: 28 September 2026 at 11:59 pm AEST
- Shortlisted applicants notified: By 25 November 2026
- Shortlisted applicant presentations: 1–2 December 2026 in Melbourne
- Program duration: Up to 24 months
- Stage 1: Approximately 4–6 months
- Stage 2: Approximately 14–18 months
- Shortlisted companies must be available to present in person in Melbourne on 1–2 December 2026. Virtual attendance cannot be accommodated.
- Register your interest with GrantHelper
ANDHealth+ objectives
ANDHealth+ aims to accelerate the commercialisation of Australian digital and connected health technologies and contribute to the objectives of the MRFF Medical Research Commercialisation Initiative.
The broader objectives include:
- Leveraging Australia’s research strengths and capabilities to improve the commercialisation and translation of medical innovations into practice.
- Bringing together funding, expertise and time required to incubate and commercialise promising innovations.
- Helping Australian innovations progress through the research and development pipeline and overcome commercialisation funding gaps.
- Attracting private capital and industry expertise to emerging Australian biomedical technology ventures.
- Developing investment-ready and enterprise-customer-ready digital and connected health SMEs.
- Improving clinical and commercial readiness.
- Supporting technologies capable of improving patient outcomes and the health and wellbeing of Australians.
- Helping SMEs achieve clinical and commercial milestones that can drive institutional investment and enterprise customer uptake.
- Accelerating market entry and growth for evidence-based digital and connected health technologies.
Projects and expenditure eligible for ANDHealth+ support
Projects should focus on developing clinical and/or commercial evidence that significantly improves an SME’s ability to commercialise its technology, raise growth capital and/or implement a market entry or growth strategy.
1. Product development
- Product verification and validation.
- End-user studies.
- UX/UI development designed to improve clinical outcomes.
- Intellectual property strategy.
2. Clinical development and outcomes
- Clinical trial planning and protocol design.
- Clinical trial or study design and execution.
- Clinical trial data analytics.
- Demonstrating efficacy in clinical or industry settings.
- Voice-of-end-user research in clinical settings.
- Clinical and commercial studies where the endpoints are highly relevant to successful commercialisation.
3. Manufacturing
- Manufacturing assessments.
- Design for manufacture.
- Scale-up manufacturing plans.
4. Commercial strategy, evidence and outcomes
- Go-to-market planning.
- Voice-of-paying-customer studies.
- Commercial pilot programs.
- Health economics assessments.
- Business validation in end-user settings.
- International market strategy.
- Health data and independent market intelligence.
- Business and financial modelling.
5. Regulatory and reimbursement
- Independent regulatory strategy and audits.
- Regulatory certification or roadmaps to certification, including TGA and FDA pathways.
- Reimbursement and pricing strategy, verification and audits.
- Cybersecurity.
- Data collection, storage, security and privacy.
- Quality Management Systems planning.
- Multi-jurisdictional compliance planning.
Ineligible expenditure and activities
Funding cannot be used for expenses that are not directly related to approved ANDHealth+ projects or for normal business operations.
Ineligible activities include, but are not limited to:
- General and administration costs relating to day-to-day business expenditure.
- Non-related staffing or contracting costs.
- Applicant staff time supporting project activities unless specifically pre-approved.
- Ongoing software and hardware development.
- Sales, marketing and branding costs.
- Fees used to incentivise customers to purchase or use products or services.
- Travel costs and associated quarantine or medical expenses.
- Government agency fees, such as ASIC fees.
- Direct patent or registration fees and licence costs.
- Activities already funded through another MRFF grant, as double-dipping is not permitted.
Project-specific employment and materials directly related to approved activities may be supported. Internal staff funding must be pre-approved and timesheets may be required.
Other ANDHealth+ important details that you will need to know
Organisations eligible for ANDHealth+ support
Applicants must:
- Be an Australian SME and registered Australian corporate entity.
- Employ no more than 199 employees.
- Meet ASIC small-business thresholds, including consolidated revenue below $50 million and/or consolidated gross assets below $25 million at the end of the previous financial year.
- Have at least one full-time employee engaged in the business.
- Have sufficient management capacity and resources to participate effectively in the intensive program.
- Have at least 6–12 months of operating runway to cover business-as-usual expenditure, with at least 12 months preferred.
- Be authorised to use all intellectual property required to undertake the project.
- Possess or control exclusive global rights to use novel intellectual property required for the project.
- Demonstrate that the primary benefits from developing and commercialising novel IP will accrue to Australia.
- Demonstrate gender diversity across the Board of Directors and Leadership team.
- Be willing to provide required outcomes data and reporting throughout the program and for three years following completion.
- Submit a fully completed application with all required attachments.
Companies with a single-gender Board or Leadership team are generally ineligible.
A stated intention to improve diversity does not satisfy this requirement, and Advisory Board members cannot be counted unless they are members of the Board of Directors or Leadership team.
Companies with up to five FTE-equivalent employees that have not established a Board of Directors are exempt from the Board diversity requirement. Other applicants must demonstrate meaningful gender diversity at both Board and leadership level.
The proposed technology must:
- Meet ANDHealth+’s definition of evidence-based digital or connected health technology.
- Align with the objectives of the MRFF.
- Have reached or substantially demonstrated proof of concept.
- Have a minimal deployable product sufficiently developed for meaningful clinical evaluation.
- Demonstrate externally validated clinical, health-system or end-user need.
- Have a pathway to a viable business or revenue model that can be independently verified.
- Be evidence-based and clearly focused on improving patient outcomes.
Eligible technologies can include software-based and software-enabled medical devices and connected medical devices where significant intellectual property and clinical benefit are incorporated into the technology.
Not-for-profit enterprises may apply if they satisfy all eligibility requirements, although ANDHealth+ is primarily designed for for-profit commercialisation-focused SMEs.
Eligible university, research institution and industry spinouts may also apply. Organisations relying heavily on a parent entity or major shareholder must demonstrate how ANDHealth+ activities will be ring-fenced from business-as-usual operations.
ANDHealth+ selection criteria
No percentage weightings are published by ANDHealth. Applications are considered across the following areas:
1. Patient value
Applicants should demonstrate:
- How the product improves diagnosis, prevention, treatment, mitigation and/or management of acute or chronic conditions.
- How these improvements ultimately deliver benefits to patients.
- Clear evidence that the technology is focused on meaningful health and clinical outcomes.
2. Understanding of end users
Applicants should demonstrate:
- A strong understanding of who will use the product and how.
- How the solution integrates into existing clinical workflows and/or patient journeys.
- A clear distinction between users, payers and beneficiaries.
- Evidence of Voice of User research and validation.
3. Uniqueness and competitive advantage
Applicants should demonstrate:
- A clearly defined problem and the specific pain points being addressed.
- Understanding of the limitations of existing solutions.
- Knowledge of current approaches used to address the problem.
- Analysis of direct, indirect and emerging competitors.
- Understanding of competitive and market forces that could create adoption barriers.
- A clear explanation of what is genuinely new and unique about the technology.
- Evidence of technological, methodological or application advancement over competing solutions.
- Superior outcomes for users and a compelling proposition for customers and payers.
- Defensible and sustainable competitive advantages.
- Barriers preventing competitors from easily replicating or superseding the technology.
- Sustainable market positioning and appropriate protection mechanisms.
4. Technology maturity
Applicants should demonstrate:
- Evidence that the technology has achieved proof of principle or proof of concept in a clinical or market environment.
- Access rights to essential data required for operation, where relevant, including AI and machine-learning training data.
- An appropriate patient data privacy and security strategy.
- Clinical evidence, including trials and technical certification where applicable.
- A considered regulatory strategy, including identification of relevant TGA regulatory classification.
- Evidence of product traction in clinical or market environments.
- Consideration of scalability barriers, including required integrations.
- Appropriate stakeholder identification and engagement.
5. Market and business case
Applicants should demonstrate:
- A feasible and credible business model.
- A strong value proposition for identified payers.
- Evidence of market demand and appetite.
- Voice of Paying Customer evidence.
- Understanding of the size and characteristics of the target market.
- A credible pathway to market.
- A clear intellectual property strategy and position.
- Understanding of barriers to market entry.
6. Team
Applicants should demonstrate:
- Commercial acumen and business development capability.
- Experience navigating healthcare markets and engaging relevant stakeholders.
- Strategic planning and execution capability relevant to digital and connected health commercialisation.
- Technical expertise appropriate to the innovation.
- Core technology development and engineering capabilities.
- Appropriate regulatory and quality assurance knowledge.
- Healthcare-appropriate product development methodologies.
- A track record of commercialising healthcare technologies or products.
- Ability to engage healthcare providers, payers and patients.
- Ability to scale operations and achieve sustainable growth.
- Diversity across the Board, Leadership team and wider organisation.
- Inclusive leadership and organisational culture.
7. Program impact and fit
Applicants should demonstrate:
- How proposed projects will materially improve the clinical readiness of the technology.
- How proposed projects will materially improve commercial readiness.
- Why participation in ANDHealth+ will accelerate the company’s commercialisation pathway.
- Why the organisation is a strong fit for the ANDHealth+ model and intensive support structure.
- A strong understanding of the complexity involved in commercialising digital and connected health technologies.
Preference is given to companies demonstrating significant understanding of the challenges associated with commercialising digital and connected health products.
How do I get the ANDHealth+?
To strengthen an application for ANDHealth+, applicants should demonstrate:
- A compelling evidence-based digital or connected health innovation with clear potential to improve patient outcomes.
- Proof of concept or proof of principle and a sufficiently mature working product.
- Validated clinical, health-system and end-user need.
- A clear understanding of the problem being addressed and weaknesses in existing solutions.
- Strong differentiation from direct, indirect and emerging competitors.
- A sustainable and defensible competitive advantage.
- Evidence of clinical or market traction, such as pilots, customers or product use.
- A credible clinical evidence strategy.
- A clear regulatory pathway and understanding of applicable TGA requirements.
- Strong data privacy, cybersecurity and quality-management considerations.
- A viable and scalable business and revenue model.
- Evidence of market appetite and Voice of Paying Customer validation.
- A credible go-to-market and growth strategy.
- A clear intellectual property strategy and sufficient rights to commercialise the technology globally.
- A capable team combining commercial, healthcare, technical and regulatory expertise.
- Appropriate gender diversity across leadership and Board structures.
- Sufficient operating runway and organisational resources to participate fully without relying on ANDHealth+ funding for normal operations.
- Well-defined Stage 1 and Stage 2 activities capable of materially improving clinical and commercial readiness.
- A clear explanation of how the proposed activities will help attract investment, secure enterprise customers or accelerate market entry.
- A strong organisational fit with ANDHealth+’s intensive, milestone-based commercialisation model.
- An understanding of the complex commercialisation pathway for digital and connected health technologies.
- Capacity and willingness to engage closely with ANDHealth, the Industry Advisory Panel and other program experts.
Information to prepare for the ANDHealth+ application
Applicants should prepare:
- Completed online application responses.
- Proposed project outline.
- Investor Pitch Deck, limited to 15 slides.
- ANDHealth Lean Canvas using the mandatory one-page landscape template supplied through the application platform.
- Product demonstration provided via a link, such as YouTube or Vimeo.
- Letter of Board Support using the provided template.
- CEO letter where the applicant does not have a Board.
- Financial forecasts covering at least three and up to five years.
- Capitalisation table identifying major and notable shareholders.
- ASIC Company Extract.
- Stage 1 and Stage 2 Project Plan Overviews using the supplied template.
- One-page Risk Register using the supplied template.
- Evidence confirming Australian SME status.
- Evidence of sufficient operating runway.
- Evidence of rights to relevant intellectual property.
- Evidence demonstrating compliance with Board and Leadership gender-diversity requirements.
- Relevant supporting documents directly related to the business and technology.
Applicants must also read and agree to the cohort company expectations document when submitting their application.
Applying for the ANDHealth+
Applications must be submitted online through the Gust application platform.
Register your interest with GrantHelper to explore your alignment with this program and how we can assist you to increase your chances of success.
ANDHealth+ resources
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