D+I is ISO 13485:2016 Certified

D+I is proud to announce that we have achieved ISO 13485:2016 certification — recognition of our commitment to design and engineering excellence in the development of medical devices.

With regulatory requirements becoming increasingly stringent, ISO 13485:2016 certification guarantees that our quality management processes meet the internationally agreed standard for the medical devices industry. D+I is one of the first product development consultancies in Australia to achieve this certification.

“D+I have been delivering complex medical devices for over 30 years. Receiving ISO 13485:2016 certification is recognition of the quality processes we have adopted at D+I and is a direct reflection of our commitment to best practice in design and engineering for the medical device industry,” says David Jones, Head of D+I.