What strict reporting does DCGI call for related to medical devices
DCGI is emphasizing strict reporting of side-effects associated with medical devices.
- DCGI (Drug Controller General of India) calls for the strict reporting of side effects associated with medical devices to ensure patient safety and monitor device performance.
- Healthcare facilities and manufacturers are required to promptly report any adverse events, malfunctions, or defects related to medical devices to the appropriate regulatory authorities.
- DCGI emphasizes the importance of maintaining a comprehensive database of adverse events to continuously evaluate and improve the safety and efficacy of medical devices.
- Timely reporting of side effects helps in identifying potential risks and implementing necessary measures to prevent harm to patients.
- DCGI also encourages healthcare professionals to educate patients about the importance of reporting any discomfort or adverse reactions they may experience while using medical devices.
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a year ago