Certified Management System

RRC is certified according to ISO 9001:2008 and ISO 13485:2007 (medical equipment manufacturers) and in addition, operates according to the principles of TQM (Total Quality Management) and FDA requirements (QSREG 820) at all locations.

Product Approvals

RRC has many years of experience in the approval of equipment during the development stage with the most important certification agencies and licensing authorities worldwide. The end-product is delivered to the customer with all desired and required agency approvals.

Quality Assurance

In addition to the standard quality assurance systems, all of our products are put through a 100% in-line functional testing. The data from this test is recorded and stored for statistic process controls and traceability in real-time.

Auditing

RRC carries out audits at its subcontractors, production plants and with its employees more often than average firms.  This is done to make sure that our high requirements on quality are adhered to. Audits from RRC's discerning customers also help to constantly improve quality. 

RoHS / Reach / WEEE

During the development stage we make sure that our products are developed and produced according to ecological methods, guidelines and norms. The materials and parts used are selected so that our products meet the requirements of the RoHS, the Reach-guidelines and the WEEE-directive.

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