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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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What is 18-cder-05-06doc - aiims?
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).
Who is required to file 18-cder-05-06doc - aiims?
Healthcare professionals, pharmaceutical companies, and drug manufacturers are required to file 18-cder-05-06doc - aiims.
How to fill out 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.
What is the purpose of 18-cder-05-06doc - aiims?
The purpose of 18-cder-05-06doc - aiims is to ensure the safety of patients by reporting and analyzing adverse drug events.
What information must be reported on 18-cder-05-06doc - aiims?
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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