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Medical Device Vigilance | MD & IVD compliance
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This introduction to medical device vigilance and incident reporting explores the mechanisms established by the European Medical Device Regulations (MDR), highlighting the processes that manufacturers and healthcare providers must follow to report adverse events and device deficiencies. Through these regulations, the EU seeks to enhance device safety and efficacy, ensuring optimal outcomes for patients and users.
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Also, Explore our latest blogs:
✆ +44 (0) 2030 626880