To ensure that the pharmacovigilance system of the company is maintained and managed.
Ensures that information concerning all Adverse effect (AE) and drugs Adverse Reaction (ADR) that are reported to the company employees is collected and collated.
Ensures that documents and products are submitted to NAFDAC and PCN.
Making Administrative payments, arrangements, preparation and submission of various documents to NAFDAC.
To ensure submission of periodic safety update report.