Central Drugs Standard Control
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Dte.GHS, Ministry of Health and Family Welfare, Government of India

 

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Pharmacovigilance Protocol
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Adverse Drug Reaction Reporting

CDSCO solicits the cooperation of healthcare professionals
in collecting data of adverse events related to drugs marketed in India. The submitted data will be collated and evaluated by the
National Pharma-co-vigilanc Center
operating at The Department of Pharmacology,
All India Institute of Medical Sciences, Ansari Nagar, New Delhi.

 

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