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Edwards Lifesciences
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Columbus, Ohio
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, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements ... medical device regulatory requirements and documents, device accountability and adverse events reporting
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Edwards Lifesciences
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Columbus, Ohio
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, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements ... medical device regulatory requirements and documents, device accountability and adverse events reporting
...
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Edwards Lifesciences
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Columbus, Ohio
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reporting executing Board materials and equity programs. Conduct competitive market analysis to establish a ...
Extensive knowledge of industry trends and regulatory changes
Stay current on industry knowledge
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