Scientific Administrator
European Medicines Agency (EMA), Netherlands
Kelly is a pharmacist with an additional master degree in medicines regulatory affairs who joined EMA in 2008. Before joining EMA, she worked in the pharmaceutical industry, mostly in pharmacovigilance. Since at EMA, she has been involved in many different projects for the implementation of the latest PhV legislation, in signal management and in RWE activities as part of the Real-World Evidence workstream in the EMA Data Analytics and Methods Taskforce. She coordinates the EMA/HMA Patient-registries initiative.
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Ensuring Patient Registries Support Regulatory Decision-Making
Wednesday, October 4, 2023
3:30 PM – 4:30 PM EDT