Akash Sharma

Gained exposure to various pharmacovigilance domains, including ICSR Processing, Aggregate reporting, Literature surveillance, Regulatory affairs, Mailbox handling and Compliance.

Gained exposure of safety database Argus and its tabs.

To have overview of SDEA process and Regulatory intelligence activity.

Gained hands-on experience in SDEA drafting, periodic Review and amendment.

AE /ADR and product list reconciliation with partners.

To check product approval, withdrawal notification received from drug safety mailbox for product approval, withdrawal.

To provide support on regional PV activities

Supported staff members in their daily tasks, reducing workload burden and allowing for increased focus on higher-priority assignments.