While the wide-ranging subject of quality is perfectly well regulated in clinical trials, it still remains foggy in observational research because of some legal gaps that lead to frequent difficulties/doubts for specialized operators. During this webinar we will explore different views on this subject, bringing some specific situations related to Real World Data research and giving much room for discussion from the audience.
Sara Montanari, MediNeos Quality Assurance Manager
She has competencies in genetics, clinical epidemiology, GCP, Patients Reported Outcomes, computer system validation, pharmacovigilance, quality assurance and quality compliance processes, and in laws and regulations applicable to the conduction of clinical studies.
Zakeria Abdi, Medineos Business Developer
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.
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Free online Webinar reserved to MediNeos clients