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.
biopharma attendees
biopharma companies
countries
customer speakers
2024 Keynotes
Advancing Innovation
in R&D and Quality
Beating the Odds to Accelerate
Cures for Rare Diseases
Product Roadmaps, Innovation Theatres, and more
Watch Now
Vault Platform
Clinical 
Quality & Manufacturing 
Safety 
Regulatory 2024 Veeva Heroes
Each year, Veeva honors industry pioneers who have gone above and beyond. These innovators pushed boundaries and navigated change in their companies to improve processes and help move the industry forward.
The Hero award recognizes forward-thinking people who have led substantial changes within their organization, resulting in exceptional outcomes across the industry.
John Reilly
Head, Veeva Center of Excellence
GSK
Accelerated R&D digital transformation by pioneering cross-functional governance and Vault management.
Pieter Voermans
Head Clinical Data Management
Sobi
Improved oversight and control through streamlined clinical data collection with global standards.
Giorgia Donati
Trial Master File Specialist
Alfasigma
Driving inspection readiness and sponsor oversight with a unified clinical operations platform.
Philippe Barrau
Digital QMS Program Leader
Sanofi
Optimized quality processes for 90,000+ users globally.
Aysegul Ozkose
Senior RA Database Manager
Nordic Pharma Group
Driving the continuous transformation of regulatory operations by adopting a unified RIM platform.
Pilar Carrero
Vice President, R&D Process Optimization
LEO Pharma
Globally streamlined safety operations and eliminated affiliate reconciliation and local logs.
Gallery
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.