About me
I am a pharmacoepidemiologist & RWE specialist within the Data Analytics and Method Taskforce at the Europea Medicine Agency (EMA). I am part of the RWE workstream that provides support on RWE related matters to different evaluation committees, delivering rapid analyses of RWD to answer regulatory related research questions. My current responsibilities include leading some RWE studies using inhouse databases or via DARWIN EU, co-leading the EMA use case within the EHDS pilot and facilitating the work around the use of patient experience data in regulatory context. My background training is in biostatistics and health economics with more than 15-years prior experience on evidence generation to support HTA and payers decision-making.
