She currently has over seven years of pharmacovigilance experience, during which she was also responsible for operational management of the pharmacovigilance clinical and post-marketing projects for number of pharma companies from large and medium to small.
During her work in pharmacovigilance, she gained experience in pre- and post-marketing case processing, aggregate report writing, preparation of safety data exchange agreements, safety management plans and standard operating procedures, preparation and maintenance of the Pharmacovigilance System Master File and GVP Auditing.
Her most recent activities included the assessment and impact of new EudraVigilance system requirements on Marketing Authorisation Holders and their PV system for ICSR management.
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