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Next Medineos webinar: "Understanding PASS studies: obligation or opportunity?" - Sept 6th

The webinar will provide an overview of the regulatory framework applicable to the conduction of an observational PASS study. Attendees will be given indications on mandatory and recommended provisions on the design of an observational PASS study.

Speakers:

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.

Click here to register

Free online webinar reserved to MediNeos clients

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