World Drug Safety Summit
World’s greatest minds in drug safety, pharmacovigilance, data analysis, reporting, government policy, and innovative technology united under the Why Summits Future of Pharmacovigilance World Tour
key information
- Location: Basel, Switzerland
- Part of the Pharmacovigilance World Tour
- June 5-6, 2025
- 9:00 - 17:30 Local Time
OUR CONFERENCE PROGRAM
KEY TOPICS
- A.I. Toolbox - adoption status in 2025 and beyond
- Discussing the real value of Patient Centric Pharmacovigilance
- Vaccine Safety moving from COVID towards innovative products
- Signal Detection and Risk management in PV
- Deep dive into compliance challenges
- Power of Intradepartmental and external collaborations
- Challenges of communication with HCPs - biggest opportunities for meaningful impact
- Clinical Safety & market access
- Future of Drug Safety Profession
- And many more...
EVENT SPEAKERS
Erika Barbarosie
Shaloo Padhi
Sandoz
Michael Forstner
SOBI
Sanjeev Srivastav
BionTech
Minhaj Obeidullah
Novartis
Petros Mavrogenis
Novartis
Yvonne Nunciu
Bayer
Luvanka Hanxhari
Novartis
Sabine Poltermann
BMS
Lisa Stagi
Roche
Santanu Mukhopadhyay
Merck
Elena Radu
Basilea Pharmaceuticals
Nicolas Perez
SwissMedic
Gurpreet Singh
IQVIA
Jeurgen Dietrich
Bayer
Julien Castera
Incyte
Marija Simic Koumoutsaris
Sandoz
Marjan Dzeparoski
Bionica
Adriano Galati
Roche
Jost Leemhuis
Roche
Sibel Guerler
BMS
Alejandra Padovani
Uniqure
Testimonials
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Check out our event overview and agenda and discover World Drug Safety Summit Basel 2025.
REGISTRATION
Conference
Ticket | June 5-6, 2025-
Access to All Conference Sessions of the 9th Annual European Drug Safety Pharma & Biotech Conference Basel
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Access to Post Conference Networking
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Conference Materials
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Includes Coffee Breaks, Snacks and Refreshments, Seated Lunch
BECOME A PARTNER
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Present on the Main Stage
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Hold an exhibit at this event
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Gain exposure through alternative partnership benefits
Event Partners
At Alwis Group, we’re pioneering AI-driven solutions for the healthcare and pharmaceutical industries. Our innovative tools are transforming pharmacovigilance, enhancing drug safety monitoring, and streamlining regulatory compliance. Our suite of products includes:
- ReTrans Enterprise: AI-powered literature surveillance
- ReTrans Extension: Browser plugin for real-time safety data analysis
- ScoMed: Intelligent medical literature scoring * ZiNex: Advanced medical document processing
- ZiQuel: AI-driven quality complaint management
- ZiTrack: Smart inbound receipt management
We’re committed to improving patient safety and operational efficiency through cutting-edge technology. Our solutions reduce costs, minimize errors, and accelerate processes, allowing healthcare professionals to focus on what matters most – patient care.
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise.
Accelerating Patient Safety: Leading with Evidence, AI and Scientific Expertise.
Biologit MLM-AI is a state-of-the-art platform for monitoring scientific literature to identify adverse events and emerging risks throughout a product’s lifecycle, from clinical development to post-marketing. Designed for teams of all sizes, it combines a flexible workflow with a unified global and local scientific database, enhanced by unique AI-driven screening and productivity tools. These features enable fast, accurate, and fully traceable results for all safety surveillance needs.
Biologit Database is a robust, continuously updated repository of scientific literature, optimised for compliant regulatory searches. It integrates global and regional sources into an intuitive interface, delivering high-quality results for monitoring adverse events and potential risks. With over 65 million entries and 40,000 new articles added daily from 120,000 journals across 170+ countries, it ensures comprehensive coverage aligned with FDA, EMA GVP and global standards.
HERAX assists life science companies digitalize their business and become more effective. This is done by assisting with selection and implementation of the right IT systems and business processes. HERAX consulting services combine Clinical Development-, Regulatory-, Quality-, and Pharmacovigilance operational knowledge, technologies, and project methodology. HERAX creates value for our clients through methodical project analysis, planning, and implementation focused on time, budget, and quality. Our experienced HERAX consultants take a value-centric approach when supporting projects and by doing so, helping our clients focus on what they do best – deliver life-changing products to patients.