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REDA Instrumente GmbH


  0049 (0) 7462 9445 0

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Firmengeschichte REDA-Instrumente GmbH
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Qualitätsmanagement
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REGULATORY AFFAIRS
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 Regulatory Affairs

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!

Get in touch with us!

We welcome your visit to the world capital of medical technology

REDA Instrumente GmbH   
Gänsäcker 34,  D-78532Tuttlingen
 

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