Ten Most Common Reasons for FDA 483 Observations and Warning Letter Citations in Medical Device Environments

November 15, 2019
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Engineering and Quality Teams in Medical Device Firms: Can We All Get Along?
Engineering and Quality Teams in Medical Device Firms: Can We All Get Along?

When a company’s product development engineers and quality professionals fail to cooperate adequately, the ...

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MasterControl eDHR™ Toolkit for Medical Device Firms
MasterControl eDHR™ Toolkit for Medical Device Firms

Address the challenges most medical device manufacturers experience during the device history record (DHR) ...