You’re invited to specialized sessions curated by regulatory experts from pharma and biotech companies.
We’re hosting Veeva R&D and Quality Summit as an online experience on October 14 to connect the industry while prioritizing the safety of our community.
Below, you’ll find a taste of Summit with highlights from the regulatory track.
Learn moreFeatured Regulatory Sessions
As an attendee, you will have access to dedicated regulatory sessions, including interactive Q&A with industry experts. Featured customer-led sessions include:
Roche’s regulatory transformation lead will share how his team is spearheading efforts to bring different regulatory functions together under a common set of modern business capabilities. Learn more about their OneRegulatory strategies and roadmap to meet both present and future patient needs.
Regulatory Transformational Lead
Senior Director, Vault RIM
Dermavant is one of the first biopharmas to publish a major NDA using Vault RIM. Join this session to hear how they managed that process using Vault Submissions Publishing and hired new strategic resources to support their growing portfolio.
Director, Global Regulatory Systems and Information Mgmt.
Regulatory Systems Analyst
Moderna worked with multiple health authorities and partners during their rapid roll-out of the COVID-19 vaccine. Learn how they shifted their health authority question management from reactive to proactive and aligned global efforts around a common goal.
Sr. Director, Global Regulatory Science Operations
Sr. Systems Engineer, Regulatory and Clinical Digital Applications and Platforms
Hear how Eli Lilly leveraged an agile methodology to decrease the time it takes to deploy Vault RIM capabilities. They’ll review how they pivoted from a traditional waterfall methodology, what worked well, and their top takeaways for others tackling a similar challenge.
Advisor, Global Regulatory Affairs
Director, Information & Digital Solutions, Global Regulatory Affairs
Vijay Reddi
Roche
Regulatory Transformational Lead
Roche: Regulatory Transformation Fireside Chat
11:30am EDT
Marc Gabriel
Veeva
Senior Director, Vault RIM
Roche: Regulatory Transformation Fireside Chat
11:30am EDT
Regulatory Track Closing Q&A with Strategy, Product & Services
4:30pm EDT
Jennifer LaFleur
Moderna
Sr. Director, Global Regulatory Science Operations
Moderna: Evolving Health Authority Query Management in a Rapid Commercialization Environment
12:30pm EDT
Maulik Mahant
Moderna
Sr. Systems Engineer, Regulatory and Clinical Digital Applications and Platforms
Moderna: Evolving Health Authority Query Management in a Rapid Commercialization Environment
12:30pm EDT
Paula Hudson
Eli Lilly and Company
Advisor, Global Regulatory Affairs
Eli Lilly: An Agile Approach to Vault RIM Deployment
1:30pm EDT
Amber Karns
Eli Lilly and Company
Director, Information & Digital Solutions, Global Regulatory Affairs
Eli Lilly: An Agile Approach to Vault RIM Deployment
1:30pm EDT
Jason Maze
Dermavant Sciences
Director, Global Regulatory Systems and Information Mgmt.
Dermavant: Transforming Submissions Publishing with Vault RIM
1:30pm EDT
Dan Gray
Dermavant Sciences
Regulatory Systems Analyst
Dermavant: Transforming Submissions Publishing with Vault RIM
1:30pm EDT
