Demonstration of the Medical Device post market Requirements
Remotely
<p>Brief:</p>
<p>• Corrective action requirements for safety alerts of medical devices</p>
<p>• Reporting and investigation requirements for incidents, adverse events of medical devices</p>
<p>• Detection and analysis requirements for safety signals of medical devices in the Post Market Phase</p>
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<p>Work Shop Link Remotely : <a href="https://sfda-sagov.webex.com/sfda-sagov/j.php?MTID=m456d0b18fa172b6da86… Here</a></p>
<p> </p>
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