21
JuneDemonstration of the Medical Device post market Requirements
Remotely
Brief:
• Corrective action requirements for safety alerts of medical devices
• Reporting and investigation requirements for incidents, adverse events of medical devices
• Detection and analysis requirements for safety signals of medical devices in the Post Market Phase
Work Shop Link Remotely : Click Here
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| To Date |
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| Workshop Type |
Public
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| Presenting Language |
English
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The workshop is over