Embase webinars
Learn Embase, your way: live webinars in English and French
Embase is the biomedical research database that researchers and regulators worldwide rely on for systematic reviews, drug safety monitoring and evidence-based research. With records updated daily and now with AI search, it helps you find what other sources miss.
Our webinar series shows you how to get the most from it. Start with the basics in English or French, then go deeper with a dedicated pharmacovigilance session.
Join Elsevier's Embase experts for hands-on sessions that take you from your first search to confident, workflow-ready pharmacovigilance monitoring.
Learn Embase, your way: live webinars in English and French
Embase is the biomedical research database that researchers and regulators worldwide rely on for systematic reviews, drug safety monitoring and evidence-based research. With records updated daily and now with AI search, it helps you find what other sources miss.
Our webinar series shows you how to get the most from it. Start with the basics in English or French, then go deeper with a dedicated pharmacovigilance session.
Join Elsevier's Embase experts for hands-on sessions that take you from your first search to confident, workflow-ready pharmacovigilance monitoring.
Fri, Nov. 06, 2026 · 10:00 am (GMT)
Agenda:
- Quelles sont les réactions indésirables signalées pour un médicament provenant d'un fabricant spécifique ?
- Comment mettre en place une alerte et assurer le suivi de la pharmacovigilance (et le comparer à celui de l'EMA) ?
- Gestion de l'ensemble du flux de travail, options de dédoublonnage et automatisation
Customer Success Manager, Elsevier
Customer Success Manager, Elsevier
Mon, Nov. 16, 2026 · 10:00 am (GMT)
Agenda :
- How to do a State-Of-The-Art review?
- What are the reported adverse device events?
- How to monitor a device (e.g., specific tradename or manufacturer) in PMS (Post Marketing Surveillance).
Customer Success Manager, Elsevier
Tue, Dec. 08, 2026 · 9:00 am (GMT)
Agenda:
- Comment réaliser une revue de l'état de l'art ?
- Quels sont les incidents signalés liés au dispositif ?
- Comment assurer le suivi d'un dispositif (par ex. nom commercial spécifique ou fabricant) dans le cadre de la matériovigilance (après la mise sur le marché) ?
Customer Success Manager, Elsevier
