She has extensive experience working with various medicinal products in a wide range of therapeutic areas. She was involved in ICSR processing, PSUR and RMP preparation and assessments, assessment of safety variations, PASS protocols, signal detection activities, and different regulatory procedures on the EU level. She is experienced in setting up different pharmacovigilance processes and client and team management.
+44 (0)1483 307920
+1 792 3740
United Kingdom (Head Office)
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