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Rs. 500/OFFICE OF THE DIRECTOR ALL INDIA INSTITUTE OF MEDICAL SCIENCES ANSARI NAGAR : NEW DELHI : 110 029 (SCHEDULED) S.NO. OF TENDER : FILE NO. 18/CDR/200506 Name of the party in whose Favor the
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This document is a form used for reporting adverse drug events to the Food and Drug Administration (FDA) under the 18-CDER-05-06 guidelines set by the All India Institute of Medical Sciences (AIIMS).
Healthcare professionals, pharmaceutical companies, and drug manufacturers are required to file 18-cder-05-06doc - aiims.
To fill out 18-cder-05-06doc - aiims, you need to provide detailed information about the adverse drug event, including patient details, drug information, and the nature of the event.
The purpose of 18-cder-05-06doc - aiims is to ensure the safety of patients by reporting and analyzing adverse drug events.
Information such as patient demographics, drug name, dose, route of administration, adverse event details, and outcome must be reported on 18-cder-05-06doc - aiims.
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