Highly experienced partners in medical device development and commercialization

 

FOCUS ON BUILDING SUCCESSFUL BUSINESSES AROUND AUSTRALIAN INNOVATION

  • FOCUS ON BUILDING SUCCESSFUL BUSINESSES AROUND AUSTRALIAN INNOVATION

    Ontogo is an independent supporter of Australian innovation with focus on building successful businesses around Australian innovation. Ontogo provides expertise in commercialising and scaling Australian Health Technology innovation locally and internationally. Ontogo's strength lies in their capability and process. They contribute unmatched expertise along with the rigorous application of our models, tools, systems and hands-on business know-how. Drawn from across the commercial spectrum, each offers unparalleled experience, expertise and capability. Ontogo works with clients to apply models, tools, systems and personal know-how developed during their hands-on business experience. Ontogo’s common goal is to see clients achieve success in the market.

 

ENHANCING COLLABORATION TO DEVELOP CUTTING-EDGE MEDICAL DEVICES

  • IDEAS INCUBATOR OF FLINDERS UNIVERSITY

    The Medical Device Partnering Program (MDPP) is an ideas incubator of Flinders University, Adelaide. The government funded MDPP fosters collaborations between researchers, industry, end-users and government and develop medical technologies with global market potential.

    MDPP’S focus is on connecting ideas and their multidisciplinary approach allows clients to leverage the best expertise, perspectives and networks. Projects that go through the MDPP Ideas Incubator have a strong commercial focus and are in response to industry-driven problems.

    MDPP’s aim is to build on the current research and manufacturing capability across the nation and develop Australia’s position as a global leader in the growing medical devices market.

    “MDPP is possibly the best model for fostering university-industry collaboration that I have encountered in an Australian University.”

    Dr Steven Farrugia (Vice President, Technology) - ResMed Ltd

 

INNOVATIVE PRODUCT DESIGN AND DEVELOPMENT FOR MEDICAL DEVICES

  • USER-CENTRIC, ONE-STOP SOLUTIONS FOR TECHNICAL NEEDS

    Sevilla Software & Product Development is founded by two award-winning academics with over a decade of research and industry experience. The company is driven by a dual mission: to enhance the usability and affordability of tech solutions and to serve impactful social causes. With a dedicated team and a user-centric philosophy, Sevilla excels in understanding the unique requirements of various industries, offering a comprehensive, one-stop solution for technological needs, from design to manufacturing.

    Sevilla’s expertise spans across biomedical devices, industrial automation, educational tools, and wearable technologies, ensuring ideas are transformed into functional, cost-effective realities.

 

INDUSTRY-LEADING QMS SOFTWARE

  • SCALE FASTER, BECOME MORE EFFICIENT AND REDUCE RISK THROUGHOUT THE PRODUCT LIFECYCLE

    Greenlight Guru provides the leading cloud-based solutions for MedTech companies to bring life-changing products to people faster, and with less risk. Greenlight Guru provides purpose-built quality management, product development, and clinical data management solutions that together help teams accelerate timelines, streamline compliance, and deliver high-quality products. With Greenlight Guru, companies across the globe are improving efficiency, speed, and quality in every aspect of their organization to get products to market faster and keep them on the market longer.

 

LEADING MEDICAL DEVICE AND PHARMACEUTICAL CONSULTANTS

  • LARGEST SPECIALISED REGULATORY COMPANY IN SOUTH EAST ASIA

    PharmOut was established in 2006 in Melbourne, Australia, and by delivering value for money and solutions quickly grew to become the region’s largest medical device and pharmaceutical consultancy firm in a very conservative, risk adverse market.

    PharmOut offers specialist consulting services to the medical device and pharmaceutical industries. As a leading and largest regulatory consultancy firm, Pharmout provides these services to those industries subject to PIC/S, European (EMA), US (FDA), MedSafe and Australian (TGA), drug and medical device regulations, such as the US FDA 21 CFR Part 820, and the ISO 13485 Quality Management System for Medical Devices and ISO 14971 Risk Management for Medical Devices.

 

Partners

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