Within RI a dedication to Quality permeates all that we do. We hold certification to ISO 9001:2008, EN ISO 13485:2012 (including CMDCAS) and Medical Device Directive 93/42/EEC as amended and are constantly striving to achieve all certifications and registrations required to sell our products in the Global Market Place. Continual evaluation of our products has led to the creation of the finest range of products on the market that clinics aspire to own and use.
RI is also committed to reducing our impact on the environment. Where possible we manufacture devices from recyclable material and our state of the art factory was specifically designed to reduce environmental waste.
RI constantly develops products to improve the ART process or simplify the administration of the
ART process. We regularly discuss new ideas with end users for their feedback in the development process.