Events

Understanding PASS studies. Methodology versus Regulatory Requirements

13 February 2020 , online @3pm (CET)

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.

Speaker: 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.

To register click here

The webinar is free and reserved to MediNeos clients