Worldwide the conditions under which medical devices may be brought to market are strictly regulated. From product development to the market launch, companies are required to achieve numerous quality and regulatory demands. Complicating this process is that regulatory conditions change constantly nationally and internationally and become more complicated. At Reda we follow the latest regulatory demands and control the processes of all departments. From product development through quality management!
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REDA Instrumente GmbH
Gänsäcker 34, D-78532Tuttlingen