Research on Chronic Diseases

Pharmacovigilance And Clinical Trials Open Access

 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. As per available reports about 45 Journals, 15 Conferences are presently dedicated exclusively to Pharmacovigilance and about 6364 articles are being published on the current trends in Pharmacovigilance. In terms of research annually, USA, India, Japan, Brazil and Canada are some of the leading countries where maximum studies related to pharmacovigilance is apprehensive with identifying the hazards whih are intiated with the pharmaceutical commodities and minimizing the hazard of any damage that may approach patients.

High Impact List of Articles

Relevant Topics in Medical