21
JuneDemonstration of the Medical Device post market Requirements
Remotely
![](/sites/default/files/2022-06/Unt2162022e.jpg)
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
من |
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حتى |
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نوع الورشة |
عامة
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لغة العرض |
الإنجليزية
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انتهى وقت ورشة العمل