Advancing Life Sciences R&D and Quality
Connect, learn, and collaborate with your peers across clinical, quality & manufacturing, regulatory, safety, and IT at the Veeva R&D and Quality Summit, Europe.
Attendance is complimentary for Veeva customers and other life science professionals.
Keynote Speakers
Christian Wittrup
Associate Director, Global IT Services & Procurement
Ascendis Pharma A/S
Sai Jasti
Head, Data Science and AI
Bayer
Marco Stöhr
Head of Global Regulatory Operations & RA Digital Innovation
Boehringer Ingelheim
Nath Huybens
Global Administration of Information Asset
iTeos Therapeutics
Thomas Senderovitz
Senior Vice President
Novo Nordisk
Maite Durrenbach
Chief Quality Officer
Sanofi
Rinat Lifshitz Shovali
Head of Systems & Innovation
Teva pharmaceuticals ltd.
biopharma attendees
biopharma companies
countries
customer speakers
Top Reasons to Attend
Learn about the trends that are shaping the future of R&D and Quality
Network and connect with over 1,000 of your life sciences peers
Gain the most value from your Veeva investment with new capabilities and insights
Discover Vault upcoming features in product roadmap sessions
Vault Platform
Clinical 
Quality & Manufacturing 
Safety 
Regulatory Learn From Inspiring Leaders
Companies of Past Speakers
Our Platinum Sponsors
Cherith Wallace
Global Quality Systems Manager
Almac Clinical Services
Cherith unified quality management operations with a single system and led a successful go-live and communications program for 3,500 users.
Katalin Schmelter
Head of Regulatory Information and Content Management
Bayer
Katalin drove the transformation of regulatory processes, and creation of the supporting data model for the Bayer community of 6000 regulatory end users.
Tony Lewis
Director, Trial Operations Product Owner
GSK
Tony oversaw migration of 1500 active studies and 6 million data records and optimized clinical operation processes with a single platform.
Pauline Pluviaud
Drug Safety Operations Manager
OM Pharma
Pauline modernized safety operations to support a more than 100% increase in case processing volume.
Emma Forrest
Head of Clinical Operations and Project Management
Recordati
Emma transformed Recordati's approach to clinical trials and move to a predominantly in-house model to manage rare disease studies and increase time to market.
Letizia Caccialupi
Global Head of CHC Quality Systems & Excellence
Sanofi CHC
Letizia simplified end-to-end quality management processes for 10,000 users.
Trevor Griffiths
Senior Director, Clinical Data Management
Syneos Health
Trevor implemented a new set of clinical data processes for a larger Sponsor FSP engagement that led to 50% faster EDC build times. In addition, he raised awareness of Vault EDC and CDB across multiple Sponsor and Conference engagements.