Pharmacovigilance


Pharmacovigilance defined as the study of activities which relate to the detection, assessment, understanding and prevention of adverse effects. Pharmacovigilance is public health function and study of monitoring the safety of medicines and taking action to reduce the risks and increase the benefits of medicines and also a key to drug safety. PV analysis evaluated in Phase I, Phase II, and Phase III a clinical trial which provides drug companies data on the safety assurance of the drug. The aim of pharmacovigilance in industrial areas are essentially the same as those of regulatory agencies; which is to protect patients from unnecessary harm by identifying previously unrecognised drug hazards, refuting false safety signals and quantifying risk to benefit.

  • Case narrative
  • Coding of adverse reaction descriptions
  • Coding of drugs
  • Case causality assessment

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19th World Drug Delivery Summit

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40th World Congress on Pharmacology and Therapeutics

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3rd World Congress on Biologics and Biosimilars

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36th Annual European Pharma Congress

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19th European Biosimilars Congress

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9th European Biopharma Congress

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3rd International Conference on Pharmacognosy

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20th World Drug Delivery Summit

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39th World Congress on Pharmacology

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6th World Congress on Rare Diseases & Orphan Drugs

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5th World Congress on Precision and Personalized Medicine

Zurich, Switzerland
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5th World Conference on Pharma Industry and Medical Devices

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