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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...Read more
Leading the way in setting a good example for environmental protection and taking on regional responsibility are important aims for Nate Rube, owner...Read more
Since September 2019, rantronik has been assisting a manufacturer of medical devices with obtaining qualifications for systems and validating...Read more
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...Read more
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