Pharmacovigilance is a scientific discipline which mainly pertains with identifying, validating, quantifying, evaluating and minimizing the adverse effects of therapeutic drugs, devices or biologics in order to increase their safety. The clinical research regulatory agencies worldwide including US FDA, Indian DCGI and EMEA etc., are strengthening the safety laws for adoption of a systematic Pharmacovigilance framework. The adverse event data generated by clinical trials worldwide is enormous and has led to the outsourcing of the Pharmacovigilance and Pharmacoepidemilogy services of the Pharma-Biotech Research and Development. This fact is compounded by the increasing number of local clinical trials has led to a spurt in the Pharmacovigilance job market in India.
The Pharmaceutical industry in India is valued at Rs. 90,000 crore and is growing at the rate of 12 – 14 % per annum. India is rapidly emerging as a hub of Global Clinical trials and a destination for Drug Discovery and Development along with for Pharmacovigilance.
1. Principles of Pharmacovigilance
2. Methodologies in Pharmacovigilance and Signal Detection
3. Pharmacovigilance Compliance and Management
4. Pharmacovigilance Reporting Systems and Tools for Management of Reports
Any science graduate
Must be completed Graduation
you need to bring
Educational Certificate Photo Copies
Certificate and Mark-sheet if qualify the final examination