Volver a Agenda
Session Chair(s)
Magnus Wallberg, MSC
Solution Architect
Uppsala Monitoring Centre, Sweden
Learning Objective : Identify at least two tools currently being used to track adverse events reporting.
Speaker(s)
Opening the WHO ICSR Database for Public Access
Magnus Wallberg, MSC
Uppsala Monitoring Centre, Sweden
Solution Architect
New FDA Tools for Adverse Event Reporting: MedWatchLearn, Mobile Technology, and Consumer/Patient MedWatch Form 3500B
Anna Fine, PHARMD, MS
National Institutes of Health (NIH), United States
Interim Director for ClinicalTrials.gov
EMA Perspective
Sabine Brosch, PHARMD, PHD, MPHARM
European Medicines Agency, Netherlands
Data Protection Officer
¿Tiene una cuenta?