ISSN: 2048-9145

Pharmaceutical Bioprocessing

Academic Pharmacovigilance And Clinical Trials Journals

 Pharmacovigilance activities related to collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products and the safety surveillance and risk management. Pharmacovigilance plays a critical role in minimizing the risk of any harm that may come to patients by safety surveillance, risk management and identifying the hazards associated with pharmaceutical products. Clinical trials is that the propagative studies conducted on patients using of patient data, disease mechanisms, therapeutic interventions and epidemiology, patient centric approach and benefit risk management. Pre-Clinical trials are essential before a corporation starts performing the clinical trials and helps in calculating toxicity, efficacy and collecting pharmacokinetic data. Pre-Clinical and Clinical Trials involve intervention of human subjects to study the cause-and-effect relationship between a medical intervention and a health outcome. The perfect outcome of clinical trials is minimizing risks; enhance benefits, and optimal use of an intervention of therapeutic drugs. Journal of Pharmacovigilance is about the adverse effects as well as medications toxicity,defence, side effects and pharmaceutical interference. Unintentional effects are common yet often times there is short of qualitative and quantitative statistics that allows for a precise estimation of the risk/benefits profile of pharmaceuticals. Advances in biomedical science have generated more new and complex medicines to treat a broader variety of diseases and conditions than ever before.  

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