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MDR conversion by rantronik

In April 2020, the European Commission agreed to postpone the coming into force of the Medical Device Regulation by one year to enable the Member...

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Donating instead of giving

rantronik supports SOS-Kinderdorf Württemberg

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rantronik expands their vehicle fleet with an electric car

Leading the way in setting a good example for environmental protection and taking on regional responsibility are important aims for Nate Rube, owner...

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MDR qualification and validation with rantronik

Since September 2019, rantronik has been assisting a manufacturer of medical devices with obtaining qualifications for systems and validating...

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Successful audit despite previous Form 483 from FDA thanks to support from rantronik

A comprehensive Form 483 following an audit conducted by the FDA can present great challenges for a business. Such was the case for one of our...

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