Brief:
- Safety alerts and field safety corrective action (FSCA) for medical devices
- Reporting and investigation of incidents, adverse events and complaints of medical devices
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Demonstration of the Medical Device Post-market surveillance Requirements
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The SFDA Organizes a Workshop entitled Development of technical regulations and speci ...
The food sector is organized by the Food and Drug Authority (SFDA), represented by the Executive Directorate of Technica ...
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The SFDA Organizes a Workshop entitled Development of technical regulations and speci ...
The food sector is organized by the Food and Drug Authority (SFDA), represented by the Executive Directorate of Technica ...
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GOOD CLINICAL PRACTICE FOR MEDICAL DEVICE CLINICAL TRIAL ACCORDING TO ISO 14155:2020
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