Medical Device Classification Training
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based in USA
, we have created a comprehensive training webinar recording CD package covering areas such as elements of 510(k ) ; The 510(k) Process: Medical Devices classification - US and EU; Post Market Surveillance; Medical Device Complaints, MDR's and ...
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based in USA
The following is a pack of 8 best-selling training CDs for regulatory professionals in the Medical Device industry. These courses provide information on how medical device companies can achieve compliance in the important stages of device development, marketing and ...
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based in USA
Medical devices cannot be shipped to Europe unless they are in full compliance with the European Medical Device Directive (MDD). The compliance requirements vary, depending on the classification of the device. It's not just the CE marking requirements that manufacturers and exporters have to ...
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based in USA
This comprehensive training package of ten courses is aimed at helping medical device companies gain a thorough understanding of the top 10 regulations that they should comply ...
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