Overview of Pharmacovigilance
Pharmacovigilance is drug safety process, it is also known as post marketing surveillance. Because at the time of clinical trials, the doses may differ from subject to subject and duration is also limited. For approval of drug product, Pharmacovigilance is necessary. In this adverse event reporting is the commonly associated. Any healthcare professional can report on this adverse event. After getting receipt or clinical study report, drug safety associate can triage the things, and information entered in database and finally reported to the drug regulatory authorities.