As you well know, designing and launching a product is not easy. That’s why many companies, even specialist medical device companies, don’t do it alone.
Here are the top three reasons our clients give for using a medical design agency to help them in their product development cycle.
For over 20 years, Design Reality has been supporting businesses all over the world. To create better products through innovative solutions.
As part of our long-term commitment to design in the medical field, we are proud to be ISO 13485:2016 certified – the internationally recognised standard for medical device quality management.
ISO 13485:2016 shows that, as a company, we can deliver regulatory compliant development programmes for medical devices to healthcare companies right across Europe.
Working with a compliant partner like Design Reality will enable healthcare and medical device companies to minimise the time and cost associated with integrating an external development partner into their own quality management systems. Furthermore, it means that the design process can proceed more rapidly. Seamlessly integrating quality management throughout every stage of the process.
For medical start-ups, we can provide an outsourced product development service too, within an integrated management programme. By working closely with our clients, we can deliver all the necessary technical filings for your new medical device to be sold in Europe.
However, our expertise are not just limited to the EU.
With regulatory compliance experience for the American, Australian, British and European markets; wherever you sell, we can help.
If you’re interested in speaking to us about the design of a medical device, and would like to take advantage of our ISO 13485: 2016 certification, please get in touch. Or meet us at Medica – 14-17 November, Dusseldorf.