Medical technology

The pace of medical technology advancements is giving rise to increased complexities such as cost challenges, evolving regulations, and a demand for novel skills. This growing momentum brings new opportunities to address critical needs in healthcare, expediting an era of preventative, curative, personalised, and decentralised care.
Realising these possibilities requires comprehensive experience in digital and physical product development. Successful delivery needs a human-centred focus, underpinned by science, and backed by experts who understand how to bring breakthrough medical technologies to market.
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Improve outcomes across the surgical care pathway through digital connectivity, advanced imaging and navigation, and wearable biosensors. We design, develop, and scale digital platforms, surgical instruments and robotics, and AI-powered tools to improve surgical care.
Accelerate launch of patient-centric drug delivery devices and combination products. We design innovative device technologies, support regulatory submissions, and help clients capitalise on market opportunities, enhance patient experiences, and stay competitive. We develop custom equipment and optimised strategies that balance cost, safety, usability, and sustainability.
Enhance diagnosis and enable timely intervention across clinical, point-of-care, ambulatory, and home-based settings. We deliver technology strategy, due diligence, regulatory strategy, sensing and assay technology invention, complex instrument and consumable development, as well as manufacturing and supply chain analysis to transform diagnostic capabilities.
Streamline the development and commercialisation of life-changing therapies through innovative technology platforms, manufacturing process optimisation, and instrument and hardware development. We create strategies and technologies to help pharma, biotech, Contract Development and Manufacturing Organisations (CDMOs), and academic centres bring advanced therapeutics to market, quicker.
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We help organisations navigate the complexities of medical technology development no matter where they are on their journey. From building product strategies and prototypes to passing regulatory hurdles, overcoming the most pressing technical issues, and launching first-to-world solutions.
Through primary research with stakeholders, monitoring industry trends, and competitive market landscaping, we determine user goals and generate insights to help you identify market opportunities and create a clear understanding of what problem to solve – ensuring your medical technology platform addresses real-world challenges, enhances patient experience, and improves healthcare outcomes.
Using a combination of design thinking, multi-disciplinary expertise, and cross-industry experience, we help you generate breakthrough solutions that meet the goals of technical feasibility, commercial viability, and user desirability, pushing the boundaries of what’s possible in medical technology.
We reduce technology and programmatic risk by rigorously testing and vetting key scientific principles and technology components and evaluating user acceptance early in the development process. Our approach includes benchtop testing and low-fidelity prototyping to verify a product’s intended functionality and design direction early in the development process.
From concept to final product, utilising a global network of design studios, research laboratories, and engineering workshops, we help you with the end-to-end development of physical and digital medical devices, systems, and platforms. Spanning design, engineering, human factors, applied science, and pilot manufacturing, we ensure that each solution is fully realised and enhances patient outcomes and user experience
Our designers, engineers, and scientists are expert practitioners of regulated medical development. Our ISO 13485 certified processes provide a robust yet flexible framework to inform our risk-based approach to design and development, enabling submission-ready design history files for new products, as well as maintaining compliance for on-market products.
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