Pharmacovigilance, also known as drug safety, is the science relating to collecting, detecting, assessing, monitoring and preventing adverse effects of pharmaceutical products, allowing us to understand more about their benefits and risks.
The aim of pharmacovigilance is to strengthen patient safety through ongoing investigations, identifying and monitoring any previously unknown adverse effects and assessing whether action needs to be taken to improve drug safety.
It is essential for ensuring that any medicines created and manufactured by pharmaceutical companies are effective and do not pose any serious danger to consumers or if they do, that they are modified swiftly and accordingly.
specialises in drug safety management, clinical trials and medical supervision.
Responsible for conducting, monitoring or reporting regular pharmacovigilance developments and supervising the processes related to ensuring drug effectiveness and avoiding adverse effects or side effects of marketed pharmaceutical products among the general population in research trials and hospitals.
A pharmacovigilance associate monitors all products and conducts post-market evaluations to ensure drug safety. These experts are actively involved in assessing adverse event writings, updating reports on safety, conducting quality and conveying drug related case reports to appropriate authorities.
Pharmacovigilance Associate plays an important role in research, development and testing of new medications in the pharmaceutical industry.
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