The webinar content spans from the main definitions of frequently used terms to the real-life examples of Observational Research deployment at various stages of the drug life-cycle. It will provide the participants with basic knowledge on ‘hows’, ‘whens’ and, perhaps most importantly, ‘whys’ of this particular kind of evidence generation.
Simona Sgarbi, Medineos Real World Data Senior Advisor
She holds a MS in biophysics. Since 2002 she has been working in MediNeos where she gained expertise in epidemiology, biostatistics, laws/regulations applied to pharmaceutical and medical devices fields as well as project management of complex multinational peri and post approval studies. She highly skilled in the design of observational studies with different study designs (prospective and retrospective cohort studies, case control, cross sectional) and various typology (Epidemiological Studies, Patient Registries, PASS/PAES, …). She is author of several scientific publications and lectures both at national and international congresses. She is an active member of different national and international scientific associations
Zakeria Abdi, Medineos Business Developer
Graduated in MSc Pharmaceutical Sciences at Aston University and BSc Medical Sciences and Pharmacology at Coventry University. After having worked in the GMP pharamceutical manufacturing industry for several years, he joined Medineos as business developer in 2017. Since then he has been involved with various stages of the development and conduction of clinical studies thanks to his skills in designing observational studies, study protocol writing, planning and implementation of statistical analysis in SAS, statistical reports and clinical reports, publication of results, and evaluation of psychometric properties of questionnaires.
Free webinar reserved to MediNeos clients
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