Supporting the Medical Industry in Limiting Time-to-Market through Innovation Capabilities and 72-Hour Concept-to-Reality Process

In the fast-paced world of medical device manufacturing, time to market is a decisive factor for success. The ability to design, manufacture, and deliver new medical devices at speed is crucial from the perspective of having an impact on patients, meeting regulatory requirements and the commercial success of a device.

Through our state-of-the-art Innovation Centres and unrivalled 72-hour concept-to-reality process, we collaborate with our medical customers to meet the critical demands of speed, precision, and innovation.

The Importance of Time to Market

In the medical industry, prototyping and testing is essential to be able to iterate over multiple concepts, finding the right design without losing too much time. The swift and efficient introduction of new devices is essential to meet urgent healthcare needs. In an industry where innovation is a continuous focus, getting a product to market before competitors can offer a substantial advantage, allowing businesses to capture market share and establish themselves as leaders in a particular field.

However, achieving a rapid time-to-market is not without challenges. Medical device manufacturers must navigate stringent regulatory requirements, ensure flawless production processes, and balance innovation with safety.

It is in addressing these challenges that our Innovation Centres play a crucial role, offering tailored support and cutting-edge technology that enables our customers to bring their concepts to life efficiently and effectively.

Accelerating Development with Precision

Our investment in our Innovation Centres, combined with the wealth of engineering and product design experience, provides us with a strong foundation to collaborate with leading brands in the medical and pharmaceutical industry, to build long term contract manufacturing partnerships.

The centres are equipped with advanced technology that allows for rapid prototyping, testing, and analysis of medical devices, ensuring that design flaws are identified and resolved early in the process. We ensure that all products and components are production ready during the testing and validation stage, helping to further decrease time to market.

72-Hour Concept-to-Reality Process: Unrivalled Speed

Rosti Group’s standout offering is its unparalleled 72-hour concept-to-reality process. In an industry where development cycles can often span months or even years, our ability to quickly turn a concept into a functional prototype is a strong support early on in the development stage.

The 72-hour process integrates rapid prototyping with injection moulding expertise, creating a seamless workflow that accelerates development. It enables us to test concepts in real-world scenarios, gather critical feedback, and make necessary adjustments almost in real-time. By significantly reducing the time between concept development and prototype testing, enabling medical device companies to meet market demands swiftly and confidently.

Supporting Regulatory Compliance and Precision Manufacturing

Precision and regulatory compliance are equally vital in medical device manufacturing. We ensure that our rapid development process adheres to the rigorous standards required for medical device manufacturing. From material selection to cleanroom production readiness, every aspect of the process is designed to meet the exacting standards set by global regulatory bodies.

Our commitment to quality is matched by our commitment to innovation. By leveraging decades of expertise and cutting-edge technology, we not only accelerate time-to-market but also ensures that each product is manufactured with the highest level of precision and safety.