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Recommendations & Regulatory actions on drugs: Based on Pharmacovigilance Programme of India (PvPI) data.

  • At: 2016 FIP Congress in Buenos Aires (Argentina)
  • Type: Poster
  • By: KUMAR, Pranay (Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Govt. of India, Pharmacovigilance, Ghaziabad, India)
  • Co-author(s): Pranay Kumar:,Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Govt. of India,Ghaziabad,India|V. Kalai selvan:,Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Govt. of India,Ghaziabad,India|Prabhakar Mishra:,Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Govt. of India,Ghaziabad,India|Ismeet Kaur:,Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Govt. of India,Ghaziabad,India|G. N. Singh:,Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Govt. of India,Ghaziabad,India
  • Abstract:

    Ministry of Health & Family Welfare, Govt. of India launched nationwide Pharmacovigilance Programme of India to monitor the Adverse Drug Reactions (ADRs) in Indian population and to provide scientific support to Central Drugs Standard Control Organization (CDSCO) to take appropriate regulatory decisions. 

    Statistical method used in the analysis of

    ..

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Last update 4 October 2019

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