Amrita Mallick

Pharasafer UK( aka CABSCI) Delhi
Pharmacovigilance associate 

 • Responsible for assessing the safety of pharmaceuticals drugs once they’re on the market. • Using standardised guidelines, they determine whether the medication causes any adverse reactions in patients and report their findings back to the pharmacovigilance department. • Worked under a very tight timeline as, as soon as an alert of a serious adverse event (SAE) is raised the clock starts and sets into motion the necessary tasks that need to be completed to process the events. Medical cases including hospitalisation, significant disability, congenital anomaly or other medically important events require this process to be completed in 2-7 days. • Seemingly linear process can be more complex than it appears when you consider that we were working on multiple projects at once, each with different Sponsors. In addition, the timelines may depend on the study specifications previously agreed on with the Sponsors, and compliance must be guaranteed

Uttar Pradesh University of Medical Sciences Safai
Bachelor of Pharmacy (GPA: 8.17)