Pharmacovigilance Good Practice Guide by MHRA,UK

Pharmacovigilance Good Practice Guide by MHRA is published by Inspections and Standards Division of the MHRA which assesses pharmaceutical companies’ compliance with UK and EU legislation which relates to the monitoring of the safety of medicinal products.

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Pharmacovigilance Explained

What is Pharmacovigilance?

Pharmacovigilance (PV) is the a science relating to the detection, assessment, understanding and prevention of adverse drug reaction or events or side effects of various pharmaceuticals drugs and medicines.

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