See You in Boston
September 9-10, 2024
Stay Informed

Agenda

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Tuesday, September 12

3:30 p.m. – 6:00 p.m.

4:00 pm - 7:30 pm

5:00 pm - 7:30 pm

Sessions
2:00 p.m.

Wednesday, September 13

9:00 a.m. – 6:00 p.m.

7:30 a.m. - 8:45 a.m.

9:00 a.m. - 10:00 a.m.

Join Veeva to explore the latest innovations in R&D and Quality, and what lies ahead for the industry. Gain insights from industry leaders Gilead and Replimune as they share strategies that better serve patients and speed access to medical breakthroughs.

Peter Gassner Veeva Systems
Founder and CEO
Avril England Veeva Systems
General Manager, Vault
James Reilly Veeva Systems
Vice President, Development Cloud Strategy
Regina Norelli Replimune
Senior Director, Clinical Data Management
Jennifer Trundle Gilead Sciences
Director, Quality Information Systems

Connect
10:00 a.m. - 10:30 a.m.

Zone Keynotes
10:30 a.m.

Join the regulatory zone keynote for exciting updates on the Vault RIM Suite, plus a fireside chat with Scott Cleve from Daiichi Sankyo. He’ll share his thoughts on the evolution of regulatory submissions from documents to data.

Scott Cleve Daiichi Sankyo
Vice President, Regulatory Operations, Information & Compliance
Marc Gabriel Veeva Systems
Vice President, Vault RIM
Eldar Curovic Veeva Systems
Vice President, Product Management Vault RIM

A top pharma quality leader breaks down the elements of driving a successful quality transformation journey across the enterprise and how it serves as a catalyst for innovation and operational excellence. Also, hear Veeva’s vision for quality, including new product announcements.

Michael Jovanis Veeva Systems
Vice President, Vault Quality & Manufacturing
RJ Doornbos Amgen
Vice President, Quality Operating System, Services and Sciences

Takeda shares its vision to deliver medicines to patients faster and their achievements towards that vision. Hear practical strategies to deliver more efficient trials and better outcomes for patients, sites, and sponsors.

Penny Carlson Takeda
Vice President, Head of Innovation & Data
James Reilly Veeva Systems
Vice President, Development Cloud Strategy

Join our zone keynote to discover the latest industry trends and perspectives shaping the future of Veeva Development Cloud and Vault Platform. To cap off the session, Bristol Myers Squibb’s global head of Veeva drug development and quality cloud will share insights on driving optimization and innovation in a multi-Vault environment.

Raghu Nandan Bristol Myers Squibb
Global Head, Veeva Drug Development and Quality Cloud
Jared Katz Veeva Systems
Development Cloud Architect, Director of Strategy
Rik Van Mol Veeva Systems
Senior Vice President, Development Cloud

Merck shares business drivers and their digital vision across safety, clinical, medical, and quality. Hear why functional areas are partnering to transform safety operations along with recent program insights, learnings, and upcoming milestones.

Cortney Gilbert Merck
Senior Director, Business System Management and Innovation, PV Operations & Global Process Enablement
Gavin Cheong Merck
Director, Strategic Programs, Merck Research Laboratories IT, Merck
John Lawrie Veeva Systems
Vice President, Vault Safety
Derek Wagland Veeva Systems
Vice President, Products, Vault Safety

11:30 a.m. - 1:00 p.m.

Hear Veeva’s vision to unify the quality ecosystem at one of its most critical decision points: batch release. Learn how to accelerate decision making by bringing together quality process, content, data, and decision makers all in one platform.

Brian Sohmers Veeva Systems
Senior Director, Product Management, Vault Quality

See the Vault Clinical Operations Suite applications in action and the value of a unified platform in this live demo.

Tom Frattarola Veeva Systems
Senior Solution Consultant, Clinical Ops

Learn how global content plans expedite core document assembly for local affiliates.

Pam Pagnotta Veeva Systems
Practice Manager, Vault RIM Services
Cindy Ling Veeva Systems
Senior Product Manager, Vault RIM Submissions

See how you can leverage Study Portal and VeevaID to securely manage external users and seamlessly collaborate across internal and external teams.

Bryan Lim Veeva Systems
Senior Product Manager
Eric Shooman Veeva Systems
Vice President, Study Portal

Learn how emerging and midsize biopharmas can implement a safety solution in two months and manage it with limited resources.

Scott Davenport Veeva Systems
Sr. Services Engagement Manager
Raj Hattarki Veeva Systems
Practice Director, Vault Safety

Organizations are increasingly replacing document-based training with diversified learning experiences. Learn how connected processes in Vault Training – combined with a variety of training types – increase efficiency while producing qualification and compliance.

Kyle Boelter Veeva Systems
Principal Consultant – Quality

The Veeva RTSM team will demonstrate how complex clinical trial supply scenarios can be managed through highly flexible supply management settings.

Jonathan Chalifoux Veeva Systems
Senior Solutions Consultant

See how active dossier helps companies maintain a list of current documents for a given product and market.

Abigail Sasdelli Veeva Systems
Team Manager, Vault RIM
Cindy Ling Veeva Systems
Senior Product Manager, Vault RIM Submissions

See how bringing together literature review, signal investigations, and aggregate reports simplifies signal management.

Eric Woolven Veeva Systems
Senior Product Manager, SafetyDocs

Sessions
1:00 p.m. - 1:50 p.m.

Hear about Roche and Veeva’s experience with the FDA’s eCTD 4.0 pilot, which ended in May 2023. They’ll share what challenges they encountered, how they achieved success, and their recommended next steps for both industry and regulators.

Peter Goodwin Genentech, a member of the Roche Group
Regulatory Data and Content Leader
Faizan Rahim Roche
Senior Manager, Regulatory Submission

Learn how Sanofi and Jazz are rolling out Submission Content Plans (SCP) to reduce dossier planning and compilation time. They’ll share about their business case, phased adoption path, tips for successful implementation, and training strategies for key stakeholders.

Gillian Gadenne Jazz Pharmaceuticals
Senior Manager, RIM
Donna Wolfington Sanofi
Associate Vice President, Head of Global Submissions Management

Hear Roche’s journey to streamline end-to-end quality management with Vault Quality Suite. Get key insights from their implementation of lean business processes and modern technology to standardize quality events and content management and improve stakeholder collaboration.

Patricia Naughton Genentech, a member of the Roche Group
Quality Director, Computer Systems Operations Chapter Lead
Parag Shah Genentech, a member of the Roche Group
Director, Digital Quality Excellence

Hear how Minaris evolved from a system migration to an overhaul of their employee engagement and qualification process. Learn how to capitalize on change, and how sophisticated curricula matrices streamline competencies across shifts, products, and sites.

Jennifer DiMinni Minaris Regenerative Medicine
Global Head, Director, GxP Training, L&D

A Vault LIMS early adopter shares their progress in building a unified quality foundation for QA and QC that meets today’s requirements and will scale efficiently in the future. Hear how digitizing QC operations with Vault LIMS will maximize the value of quality, modernize and improve end user experience, and lower total cost of ownership.

Andrew Laughhunn Forge Biologics
Senior Director, Quality Control
Jason Boyd Veeva Systems
Senior Director, Vault LIMS Strategy

Leaders at Xencor and Kura Oncology share how they manage sponsor-owned eTMF systems and collaborate with CRO partners. This includes how to improve existing Vault eTMF implementations, develop effective and clear oversight metrics, and more.

Carolyn Jin Kura Oncology
Director, Clinical Systems and Document Management
Colin Noble Xencor
Senior TMF Systems Administrator

Haleon will share how they implemented the Veeva Development Cloud after completing a divestiture. They’ll review how they untangled their technology landscape, optimized processes on a new system, and built a partnership for strategic growth.

Mary Ann Petty Haleon
Systems, Data, and Processes Lead

Bayer shares details about their phased rollout of Vault CTMS, considerations when adding CTMS to an existing Vault eTMF deployment, and lessons learned.

Emma Earl Bayer
Head of Systems Support

Hear directly from clinical sites about the trial supply pain points they experience and what sponsors and technology providers can do to alleviate burden.

Viviënne van de Walle PT&R
PI / CMO
Valrie Patterson University of South Alabama
Clinical Research Nurse

Learn how Lilly’s standards-driven approach enables them to collect, aggregate, clean, and transform clinical trial data for dozens of studies per year, while benefiting from efficient workflows, automation of data checks across all sources, and delivery of just-in-time data.

Jenn Showalter Eli Lilly and Company
Advisor, Clinical Data Strategist
Sharon Klein Eli Lilly and Company
Director, Clinical Results Systems
Drew Garty Veeva Systems
Chief Technology Officer, Vault CDMS

UCB shares their vision for Human-Centric Health that educates, empowers and enables all to actively participate in clinical research and benefit throughout the various stages of one’s health journey. Learn how an enterprise-wide ePRO solution was a key step to reduce burden on patients, caregivers, and sites while improving data quality, availability, and transparency for study teams.

Stayce Murray UCB
Head of IT Digital Clinical Development
Seb Moity UCB
IT Lead Digital Clinical Solutions
Andrew Rohrbaugh Veeva Systems
General Manager, ePRO & eClinRO
Michelle Marlborough Veeva Systems
Senior Vice President, Product Management, Sites & Patients
Kyle Stephenson Veeva Systems
Director of Product Management, ePRO & eClinRO

Teva will discuss strategies and experiences from preparing their organization for upcoming global Vault Safety go-live. They’ll review lessons learned and recommendations for business readiness planning, process definition, data migration, training, and change management.

Rinat Lifshitz-Shovali Teva
Head of Systems & Innovation
Mike Kruczek Veeva Systems
Senior Director, Vault Safety Strategy
Melissa Aron Veeva Systems
Vice President, Vault Safety Services
Basvaraj Pinna Jeev Lifeworks LLP
Head of Engineering

Hear about Teva’s journey from a de-centralized eTMF, to Vault eTMF, and finally to a combined Vault eTMF/CTMS solution. Along with Daelight Solutions, they’ll share key program drivers, details on their technical approach, and how they applied creativity throughout the project to achieve success.

Ann O’Heney Teva Pharmaceuticals
Senior Director, Clinical IT R&D Lead
Dan Wheeler Daelight Solutions
Founder & CEO

Connect
2:00 p.m. - 2:50 p.m.

Discover how to gain full control over your requirements, ensuring efficiency, accuracy, and traceability throughout your validation lifecycle with Validation Management.

Ruben Gottardi Veeva Systems
Senior Solutions Consultant, Vault Validation Management

See how Veeva’s newest application, Link SiteBase, improves site identification and speeds enrollment with accurate real-time site data.

Jennifer Stacey Veeva Systems
Vice President, Strategy, Link Clinical
Rylan Collins Veeva Systems
Head of R&D Business Consulting, North America

See how continuous publishing streamlines activities across the Vault RIM suite.

T.J. Hynes Veeva Systems
Practice Manager, Vault Submissions Publishing
Mary Anne Potok Veeva Systems
Product Expert, Submissions, Archive and Publishing

Discuss best practices for audit readiness and working with outsourcing partners to improve oversight and data visibility.

Christina Kim Veeva Systems
Senior Director, Vault Safety

See how uploading documents and creating data in your Vault can be as easy as sending an email.

Graham Gelwicks Veeva Systems
Director, Product Management, Vault Platform

Join this discussion on improving operating models in data management — including lessons learned from Vault EDC adoption, approaches for in-house and outsourced studies, and advice for improving efficiency at organizations of all sizes.

Meg Richie Atorus Research
Vice President, Clinical Data Management
Tanya du Plessis Bioforum the Data Masters
Chief Data Strategist and Solutions Officer
Armand Matejunas Pacira BioSciences
Senior Director, Clinical Data Operations
Jon Young Veeva Systems
Director, Vault CDMS Strategy

See a demo of how to establish real-time visibility into health authority approvals and speed change control and variation management processes with the Vault Quality to RIM Connection.

Harshad Kamble Veeva Systems
Solution Consultant, Quality

Learn about all the new feasibility features we’ve delivered in Vault Study Startup to make it easier than ever to identify and select sites.

Anusha Shetty Veeva Systems
Director, Strategy, Study Startup
Erita Rothschild Veeva Systems
Product Manager, Clinical Operations

Learn how to automate correspondence with health authorities to drive faster, more compliant submissions.

Rich Merrick Veeva Systems
Senior Director, Product Management, Vault RIM

See how to streamline adverse event management and eliminate data reconciliation by bringing together clinical, safety, quality, and regulatory applications with Veeva Development Cloud.

Marius Mortensen Veeva Systems
Vice President, Product Management, Vault Safety Suite

Sessions
3:00 p.m. - 3:50 p.m.

Hear how Eli Lilly and Novo Nordisk transitioned from legacy systems to Vault Submissions Publishing. They’ll share lessons learned from three large and complex submissions, including how they updated their publishing processes to reduce submission timelines.

Tina Fuson Eli Lilly and Company
Senior Manager, Regulatory Affairs
Dionna Scott Novo Nordisk
Submission Manager, Regulatory Operations
Tiffany Chamberlain Novo Nordisk
Manager, Regulatory Operations

CSL shares best practices and lessons learned from establishing a unified quality ecosystem that harmonizes quality management business processes and centralizes millions of controlled documents to improve collaboration across business units. Learn how they are advancing their “Jobs To Be Done” vision for end to end batch release and complaints by bringing together manufacturing, quality and regulatory operations.

Rynita Julien CSL
Senior Director, Information Technology
Vasilis Mavrogenis CSL Behring
VP Of Quality

Madrigal shares their holistic quality transformation journey, including their justification for modern cloud solutions. Learn best practices, lessons learned, and how the transformation has improved quality culture, efficiency, and visibility.

Nicole Pederson Madrigal Pharmaceuticals
Vice President, Quality Assurance
Achim Schultze Madrigal Pharmaceuticals
Executive Director, GMP Quality Assurance

The current technology challenges that research sites face are compounding their even bigger business problems like an increasing volume of trials, highly complex study designs, a shrinking site workforce and a shortage of operating funds. In this session, leading site experts share their challenges and insight. Learn what they need from technology to operate more efficiently and build better partnerships with their sponsors.

Viviënne van de Walle PT&R
PI / CMO
Tina Bowdish Vanderbilt-Ingram Cancer Center
Senior Director, Clinical Research Administration
Bree Burks Veeva Systems
Vice President, Strategy, Site Solutions

BeiGene and Janssen discuss how they develop new operating models supported by eTMF innovations. They’ll also analyze how new regulations and inspection trends are shaping TMF management.

Jamie Toth BeiGene
Senior Director, TMF Management & Records
Heather Frankhouser Janssen
Associate Director, Clinical Trial Management Solutions

In this interactive session, Cerevel shares how they eliminate manual study training processes and improve compliance with Vault Study Training. They will detail how they built their business case, as well as lessons from implementation and go-live.

Grace DaFonseca Cerevel Therapeutics
Manager, Quality Operations

Astellas, GSK, Regeneron, Takeda, and Vertex will share how they are each developing Veeva centers of excellence. You’ll hear strategies for implementing a new function, getting stakeholders on board, and outlining an operating maturity model to guide the overall Veeva Development Cloud journey.

Abhishek Miglani Astellas
Director Information & Systems Strategy
John Reilly GSK
Head R&D Development (Veeva) CoE
Jennifer Grant-Hyman Regeneron
Associate Director
Guillaume Pasquier Takeda
Head Development Technology
Benjamin Zwirn Vertex Pharmaceuticals
Director, Business Engagement & Technology – Clinical Systems
Rylan Collins Veeva Systems
Head of R&D Business Consulting, North America

Improve visibility into operational processes, application usage, and KPIs with advanced Vault reporting and dashboards. Get a demo on leveraging core and new capabilities to turn ideas into actionable dashboards, and learn about upcoming enhancements.

Graham Gelwicks Veeva Systems
Director, Product Management, Vault Platform

Fortrea shares their experience with implementing Veeva RTSM, including reasons for adoption, collaboration on solution design and how this has helped overcome integration challenges and data errors.

Bireshwar Saha Fortrea
Head of Global Programming and Analytics
Dilliraja Purushothaman Fortrea
Principal Programmer
Natalie Townsend Veeva Systems
Vice President, Strategy, Veeva RTSM
Elizabeth Kreisler Veeva Systems
Senior RTSM Project Manager

Seagen and Merck join Veeva’s head of global quality services to discuss best practices for managing Vault implementations post-go-live. Learn how to systematically manage new releases, build a robust roadmap to realize the value of new features, establish governance within quality and other domains, and effectively engage Veeva for support.

Eva Sauerova Merck
IT Quality Director
Badri Devuni Seagen, Inc.
Senior Director, IT

Learn why AbbVie decided to update their clinical data technology, and how they were able to fully implement the new system in just six months.

Sanjay Bhardwaj AbbVie
Global Head, Clinical Technology Strategy and Operations
Lance Kupka Abbvie
Director, Clinical Data Systems (EDC & IRT)
Julian Rimmer Abbvie
Director Information Research
Faisal Sufi Veeva Systems
Senior Director, CDMS Strategy

Customer panel of emerging biopharmas discuss real-time data visibility and easier CRO collaboration with Vault Safety. Learn how they’re reducing operational overhead with greater control and oversight and better prepared for audits and inspections.

Joseph Wong Amylyx Pharmaceuticals
Head, PV Operations and Alliance Management
Christina Kim Veeva Systems
Senior Director, Vault Safety
Hanssar Chacon CRISPR Therapeutics
Sr. Director, Global PV and Risk Management Operations

Learn how Gilead achieved simplicity and data consistency in their RIM landscape by focusing on Vault Registrations as the first step in their journey. They’ll also share information about their cross-functional collaboration model as the key to this transformation.

Stephani Berger Gilead Sciences
Director, Regulatory Affairs CMC
Fabio Fernandes Gilead Sciences
Senior Director, Regulatory Systems

Connect
4:00 p.m. - 4:20 p.m.

See how Vault LIMS eliminates stand alone Lab Execution Systems (LES) and QC Electronic Lab Notebook (ELN) applications, simplifying the QC technology landscape and streamlining test execution to increase right first time.

Justin Lavimodiere Veeva Systems
Senior Director, Vault LIMS

Come see how Site Connect will make it possible to exchange trial information with ALL your clinical research sites.

See how Vault Registrations users can handle bulk data creation for their global product portfolios.

Nick Tasse-Guillen Veeva Systems
Principal Product Manager, Vault Registrations & MedTech
Mary Gallagher Veeva Systems
Practice Manager, Vault RIM

Join us for an industry discussion on approaches for RMP program and aRMMs tracking. We’ll discuss key requirements, planning considerations, and implementation strategies.

Grishma Sharma Accenture
Managing Director
Mike Kruczek Veeva Systems
Senior Director, Vault Safety Strategy
Eric Woolven Veeva Systems
Senior Product Manager, SafetyDocs
Devante Bignall Accenture
Management Consultant

See how to efficiently manage key GCP deviations, when identified as part of conducting a clinical trial, with Vault Quality-Vault Clinical Operations and Vault Clinical Operations-Vault CDMS Connections.

Steve Snow Veeva Systems
Product Manager, Vault QMS
Ryan Kimble Veeva Systems
Senior Product Manager

Sessions
4:30 p.m. - 5:20 p.m.

Learn how Atara and Krystal Bio leveraged Vault Submissions Publishing to bring breakthrough products to market. They’ll discuss how they transformed their traditional process, prepared for their Vault Submissions Publishing implementation, and developed best practices to maximize value.

Matt Neal Atara Biotherapeutics
Senior Director, Global Regulatory & Quality
Christopher Doan Atara Biotherapeutics
Senior Manager, Regulatory Affairs Operations
Rachael Borromeo Krystal Biotech
Senior Director, Regulatory CMC and Operation

Arcus Biosciences is transforming its computer system validation program with Vault Validation Management to improve efficiency and audit readiness. Motivated by the desire to unify and automate their quality processes onto a single platform, hear about their journey through early adopter success and the drive for incremental change.

Mike Tarsa Arcus Biosciences
Senior Director, IT Quality Security and Compliance
Venkat Prathivada Arcus Biosciences
Manager, IT Validation

AmplifyBio shares their journey to build a robust quality management system with standardized processes supported by modern quality systems. Hear best practices and lessons learned for establishing new quality processes, streamlining existing processes, or harmonizing across the organization and GxP disciplines to optimize use of digital systems.

Christina Garcia AmplifyBio
System Administrator
Claire Freitag AmplifyBio
Director, Quality Assurance
Ryan Bridenstine AmplifyBio
Quality Systems Supervisor

Learn to establish real-time visibility into health authority approvals and speed change control and variation management processes. Gilead shares its approach and best practices for building bi-directional information flow across quality and regulatory teams and connecting people, processes, and technology.

Justin O’Keefe Gilead Sciences
Senior Manager, Quality Information Systems

Learn how Amylyx shifted to managing their data in-house during a period of rapid growth. They’ll review strategies tailored to emerging biopharmas that want to get started with Veeva Development Cloud.

Wade Harwick Amylyx Pharmaceutical, Inc
Head, Global Business Applications
Allison Lusis Amylyx Pharmaceuticals
Lead, Regulatory Affairs Strategy

Hear how Veeva is connecting product data across the Development and Commercial Cloud to support cross-Vault business process. Sarepta Therapeutics will also share how they’ve used the Vault Quality to RIM Connection to date to drive more efficient change control operations and what future benefits that connected product data will provide.

John Tanner Veeva Systems
Senior Product Manager, RIM
Wim DHaeze Sarepta Therapeutics
Senior Director, Global Regulatory Operations, RIMS/DMS Lead
Tammy Griffin Sarepta Therapeutics
Director, Global GxP Quality Systems

AstraZeneca shares how their eTMF innovations drive efficiencies from study start-up to archival. Learn how to identify and implement new programs to improve document processes and become a more data-driven organization.

Sara Kraft AstraZeneca
Transformation Director

Learn how ImmunityBio leverages Vault Clinical Operations Suite to run studies for the next generation of immunotherapies. Hear why they implemented Vault eTMF, Vault CTMS, and Vault Payments at once, lessons learned, and the value of unifying as an emerging biotech.

Paula Bradshaw Immunity Bio, Inc
Vice President, Clinical Business Operations

Fortrea shares their study start-up operating model, implementation approach, lessons learned, and cycle time reductions with Vault Study Startup.

Jo Dharia Fortrea
Associate Director, Business Transformation
Patty Openshaw Fortrea
Associate Director, Clinical Systems Operational Support
Dana Glisson Fortrea
Global Head of Site Readiness and Regulatory

Join this interactive discussion to explore the trends shaping QC and how holistically transforming quality across QA and QC enables proactive quality. Hear and share best practices on forming a transformation strategy to establish an end-to-end quality foundation and maximize the value of quality.

Jason Boyd Veeva Systems
Senior Director, Vault LIMS Strategy
David Levy Scitara Corporation
Vice President, Strategy and Partnerships
LaToya Lee Jones Clarkston Consulting
Partner
Sriram Ananthanarayanan Moderna
Director, Digital QC

Join Veeva strategy and product experts to hear our clinical data vision and see an end-to-end digital trial demo — using Veeva Vault EDC, Veeva CDB, Veeva RTSM & Veeva ePRO.

Richard Young Veeva Systems
Vice President, Strategy, Vault CDMS
Andrew Gebbie Veeva Systems
Principal Solution Consultant, Clinical Data
Bipin Patel Veeva Systems
Senior Solution Consultant, Clinical Data

Join our fireside chat to hear how AbbVie eliminated multiple safety databases with Vault Safety and is implementing Vault SafetyDocs for global PSMF and risk management.

Patrick (Pat) Spracklin AbbVie
Senior Director, Strategic Operations
Sandra Strauss AbbVie
Senior Director. IT – Safety, Quality, and Medical Affairs Solutions
Mike Kruczek Veeva Systems
Senior Director, Vault Safety Strategy

Hear how AstraZeneca built support for their digital regulatory transformation with strategic alignment, organizational benefits, change management, and stakeholder management. They’ll be joined on stage by the Veeva Business Consulting team who will share how to measure delivered value against the business case.

David Berglund AstraZeneca
Executive Director, Global Regulatory Operations
Kim Brownrigg Veeva Systems
Practice Manager, Regulatory Business Consulting

Evening Event
5:30 p.m. - 9:00 p.m.

Thursday, September 14

9:00 a.m. – 3:50 p.m.

7:30 a.m. - 8:45 a.m.

See how continuous publishing streamlines activities across the Vault RIM suite.

T.J. Hynes Veeva Systems
Practice Manager, Vault Submissions Publishing
Mary Anne Potok Veeva Systems
Product Expert, Submissions, Archive and Publishing

See how Vault Glossary gives users quick and easy access to compliant, approved definitions of key terms from within the document viewer, without having to put terms and definitions into document content.

Jessica Kelley Veeva Systems
Product Expert, Vault QualityDocs
Michael Ferrell Veeva Systems
Product Expert, Vault Platform

Network with CROs and service providers to learn ways sponsors collaborate and maintain oversight with Vault Safety.

Christina Kim Veeva Systems
Senior Director, Vault Safety

Hear Veeva’s vision to unify the quality ecosystem at one of its most critical decision points: batch release. Learn how to accelerate decision making by bringing together quality process, content, data, and decision makers all in one platform.

Brian Sohmers Veeva Systems
Senior Director, Product Management, Vault Quality

See how Vault Study Training brings sponsors, CROs, and research sites into a single platform to streamline and automate study training. This includes a training plan matrix to quickly assemble training needs by role and eliminate non-compliant and manual solutions.

Shad Ayoub Veeva Systems
Senior Director, Study Training
Kelsey Donegan Veeva Systems
Solution Consultant

See how Vault Safety automates intake, case processing, ICSR submissions, and periodic reports with auto-coding, auto-translations, touchless case processing, and other innovations.

Scott Immel Veeva Systems
Principal Solutions Consultant, Safety

Learn how to shorten submission timelines by linking compliance package generation in Vault PromoMats to Vault Submissions.

Radha Maharaj Veeva Systems
Product Manager, RIM-PromoMats Connection
T.J. Hynes Veeva Systems
Practice Manager, Vault Submissions Publishing

Roadmaps
9:00 a.m. - 9:50 a.m.

Hear how Veeva is innovating to continue to unify quality processes across people, partners, and systems. You’ll learn what’s next for Vault Quality Suite and how we’re elevating quality beyond compliance.

Michael Jovanis Veeva Systems
Vice President, Vault Quality & Manufacturing
Nima Shah Veeva Systems
Vice President, Product Management, Vault Quality & Manufacturing

Explore what’s new with Vault Platform and Veeva Development Cloud. We’ll review how upcoming releases will help organizations improve scalability, user productivity, and operations. Plus, we’ll explore what’s on the roadmap for Vault Connections.

Andy Han Veeva Systems
Vice President Product Management, Vault Platform & Technology
Jared Katz Veeva Systems
Development Cloud Architect, Director of Strategy
Michael Ferrell Veeva Systems
Product Expert, Vault Platform

Hear about recently released features and the roadmap for Vault Clinical Operations Suite. We’ll share our plans to help clinical teams streamline processes, manage global disclosures, automate training across all study partners, and more.

Tom Dekker Veeva Systems
Vice President Product Management, Vault Clinical Operations
Annie Linker Veeva Systems
Product Manager, Clinical Operations
Brian Bialkowski Veeva Systems
Director, Product Management, Clinical Operations

Learn how Veeva is bringing innovation to RTSM. Hear about our overall strategic vision and roadmap for this mission critical product and ask the Veeva RTSM leadership team questions during an interactive Q&A.

Lee Gamble Veeva Systems
Director, Product Management Veeva RTSM
Steve Simmerman Veeva Systems
General Manager, Veeva RTSM

Hear the latest product updates to the Vault RIM Suite, including new roadmaps for Vault Registrations, Submissions, Submissions Publishing, and Submissions Archive.

Eldar Curovic Veeva Systems
Vice President, Product Management Vault RIM
Rich Merrick Veeva Systems
Senior Director, Product Management, Vault RIM
Kelly Finlan-Dansbury Veeva Systems
Product Manager, Vault Registrations
Lisa Musick Veeva Systems
Senior Product Manager
Cindy Ling Veeva Systems
Senior Product Manager, Vault RIM Submissions
Vera Lvovich Veeva Systems
Senior Product Manager, Vault RIM Submissions Archive
Nick Tasse-Guillen Veeva Systems
Principal Product Manager, Vault Registrations & MedTech
John Tanner Veeva Systems
Senior Product Manager, RIM

Learn what’s next for Vault CDMS, including upcoming innovations and enhancements coming to Vault EDC and Veeva CDB this year. Plus, ask the Veeva team questions during an interactive Q&A.

Drew Garty Veeva Systems
Chief Technology Officer, Vault CDMS
Raymond Letulle Veeva Systems
Senior Vice President, Products, Vault CDMS

Learn about the innovations and enhancements coming to Veeva ePRO and eClinRO, and ask the Veeva team questions during an interactive Q&A.

Michelle Marlborough Veeva Systems
Senior Vice President, Product Management, Sites & Patients
Kyle Stephenson Veeva Systems
Director of Product Management, ePRO & eClinRO

Get an overview of the Vault Safety Suite product roadmap and recent top features. We’ll share automation enhancements to speed up case processing and our vision for connecting safety to other functional areas such as regulatory and clinical.

Marius Mortensen Veeva Systems
Vice President, Product Management, Vault Safety Suite
Derek Wagland Veeva Systems
Vice President, Products, Vault Safety
Asi Roll Veeva Systems
Director Product Management, Vault Safety
Eric Woolven Veeva Systems
Senior Product Manager, SafetyDocs
Tristram Liddiard Veeva Systems
Director Product Management, Vault Safety

Connect
10:00 a.m. - 10:50 a.m.

Hear about new innovations in Vault Quality Suite to help accelerate and streamline change controls.

Glen DeGuzman Veeva Systems
Senior Solution Consultant, Quality

Get all of your roadmap questions answered by our product team in this open Q&A session.

Tom Dekker Veeva Systems
Vice President Product Management, Vault Clinical Operations
Annie Linker Veeva Systems
Product Manager, Clinical Operations
Brian Bialkowski Veeva Systems
Director, Product Management, Clinical Operations

Get an overview of the Vault Safety Suite product roadmap and recent top features. We’ll share automation enhancements to speed up case processing and our vision for connecting safety to other functional areas such as regulatory and clinical.

Marius Mortensen Veeva Systems
Vice President, Product Management, Vault Safety Suite
Derek Wagland Veeva Systems
Vice President, Products, Vault Safety
Asi Roll Veeva Systems
Director Product Management, Vault Safety
Eric Woolven Veeva Systems
Senior Product Manager, SafetyDocs
Tristram Liddiard Veeva Systems
Director Product Management, Vault Safety

Hear the latest product updates to the Vault RIM Suite, including new roadmaps for Vault Registrations, Submissions, Submissions Publishing, and Submissions Archive.

Eldar Curovic Veeva Systems
Vice President, Product Management Vault RIM
Rich Merrick Veeva Systems
Senior Director, Product Management, Vault RIM
Kelly Finlan-Dansbury Veeva Systems
Product Manager, Vault Registrations
Lisa Musick Veeva Systems
Senior Product Manager
Cindy Ling Veeva Systems
Senior Product Manager, Vault RIM Submissions
Vera Lvovich Veeva Systems
Senior Product Manager, Vault RIM Submissions Archive
Nick Tasse-Guillen Veeva Systems
Principal Product Manager, Vault Registrations & MedTech
John Tanner Veeva Systems
Senior Product Manager, RIM

Explore what’s new with Vault Platform and Veeva Development Cloud. We’ll review how upcoming releases will help organizations improve scalability, user productivity, and operations.

Andy Han Veeva Systems
Vice President Product Management, Vault Platform & Technology
Jared Katz Veeva Systems
Development Cloud Architect, Director of Strategy
Michael Ferrell Veeva Systems
Product Expert, Vault Platform

Ask the Veeva team questions about upcoming enhancements and innovations during an interactive Q&A session.

Drew Garty Veeva Systems
Chief Technology Officer, Vault CDMS
Raymond Letulle Veeva Systems
Senior Vice President, Products, Vault CDMS

We’re excited to showcase our new data applications that enable sponsors and CROs to optimize trial designs with competitive protocol design intelligence and improve site identification with real-time site data. Hear our vision and roadmap for Link TrialBase and Link SiteBase and get your questions answered.

Jennifer Stacey Veeva Systems
Vice President, Strategy, Link Clinical

Hear how Amylyx uses process navigator for more than just intuitive content navigation. Come discover the creative ways this can serve as a foundational tool for managing your quality program.

Jeremiah Genest Amylyx Pharmaceuticals
Head of Quality Management Systems

See how Vault CTMS helps you effectively demonstrate oversight with site communication logs, closed-loop issue management, real-time reports and dashboards, and more.

Mollie Gaede Veeva Systems
Senior Solution Consultant, Clinical Operations

See how bringing together literature review, signal investigations, and aggregate reports simplifies signal management.

Eric Woolven Veeva Systems
Senior Product Manager, SafetyDocs

Sessions
11:00 a.m. - 11:50 a.m.

Hear how Roche is bringing together regulatory data and processes into a single, end-to-end approach. They’ll share how they are actively evolving toward a transformative state that prioritizes data-driven decisions to move the business forward.

Daniela Trogolo Roche
RIM Process Lead
David Cook Roche
Senior Business Systems Lead

Join this interactive session to see demos of the latest advancements in Vault QualityDocs and Vault Station Manager, including External Collaboration for Documents, QR Code Generator, and more. You will also hear what’s next on the roadmap and get your questions answered.

Stephen Chelladurai Veeva Systems
Director, Product Management

Hear Veeva’s vision and roadmap for Vault QMS. Get demos of recent innovations and hear what’s next on the roadmap around topics such as intelligent automation, audits and inspections, and quality risk management (QRM). Also, Veeva’s product experts will answer your questions in this interactive session.

Manaphan Huntrakoon Veeva Systems
Senior Director, Vault Product Management, QMS
Prannoy Kothari Veeva Systems
Senior Product Manager, VPS, QRM, and MedTech Quality

Hear Vault Training’s roadmap and vision, see demos of the latest innovation, and get your questions answered. Highlights will include the enhanced experience for learners, curriculum completion data, and efficient ways to manage your training matrix.

Joby George Veeva Systems
Director, Product Management
Erin Coppola Veeva Systems
Senior Product Manager, Vault Training

Gain insight into how Vault LIMS is modernizing the QC lab to maximize right first time while improving efficiency and visibility. Get a demo of the latest capabilities, including sample management, test execution, instrument integrations, and review by exception and learn about the future vision and roadmap including a first look at stability study management.

Jason Boyd Veeva Systems
Senior Director, Vault LIMS Strategy
Nima Shah Veeva Systems
Vice President, Product Management, Vault Quality & Manufacturing

Learn what tools and resources are available for Vault Admins and Developers to solve complex use cases with Vault Admin UI, Vault API, and Vault Java SDK. We’ll also review features that help customers automate deployments, integrate systems, and extend the Vault Platform.

Mark Arnold Veeva Systems
Director, Product Management, Vault API & SDK
Eric Matelyan Veeva Systems
Associate Developer Support Engineer

GSK will share how they grant system access based on HR-designated roles and study team assignments. They’ll also explain how they authenticate sites through internal active directory and SSO, and how they plan to incoporate VeevaID into their provisioning.

Brian Grant GSK
Veeva CoE Service & Strategy Lead
Vinay Kumar GSK
Product Director, Site Engagement & UAM

Takeda shares their clinical trial management transformation approach and the value they’ve realized to help them deliver medicines to patients faster. Hear about critical aspects of their technical and organizational readiness workstreams – from business process design to change management, communications, and end user adoption.

Claudine Guild Takeda
Senior Manager, Process, Training, and Digital Solutions
Nick Kurkjy Takeda
Product Lead, Clinical Trial Management
Nathan Thomas Veeva Systems
Team Manager, R&D Business Consulting

Learn about AbbVie’s vision for improved site collaboration, and their use of Veeva products to simplify site document exchange, guarantee safety letter distribution, and improve study quality. You’ll also hear about best practices and lessons learned along the way.

Kenny Kong Veeva Systems
Vice President of Strategy – Site Connect
Karen Whitson AbbVie
Associate Director, Study Start Up Operations

Nick Darwall-Smith leverages their extensive experience in clinical trial supply to discuss how connected RTSM solutions can drive study efficiencies and explores future opportunities for innovation.

Nicholas Darwall-Smith NDS Consulting
Owner
Natalie Townsend Veeva Systems
Vice President, Strategy, Veeva RTSM

See how Moderna globalized PSMF management leveraging core Vault SafetyDocs capabilities in less than 4 months. Seamlessly collaborating cross-functionally and with external reviewers and contributors, the QPPV team reduced overhead to manage and maintain specific content for local / regional requirements. They automated logbook generation, have real-time oversight, and can more easily deliver a high-quality PSMF.

Marc Nephtali Moderna
Senior Director Digital PV and Clinical

Learn how Boehringer Ingelheim is engaging with sites and patients not only to address their needs in trial design and conduct but also to inform the BI digital transformation efforts and change management practices. Hear best practices from their journey and why creating meaningful strategic goals and relationships are fundamental to successfully embedding patient and site engagement practices across organizations.

Tracey Robertson Boehringer Ingelheim Pharmaceuticals inc.
Head of Patient & Site Engagement Capabilities
Andrew Rohrbaugh Veeva Systems
General Manager, ePRO & eClinRO

Alcon shares how a unified clinical data management approach reduces manual effort and ensures analysis-ready data at all times. Learn about Alcon’s journey to adopt modern approaches to support the development of clinical trial designs that capture a wide variety of modern data sources.

Leianne Ebert Alcon
Head of Clinical Data Operations
Richard Young Veeva Systems
Vice President, Strategy, Vault CDMS

In this two part session, AstraZeneca will share how they established new data management principles for global and affiliate markets as part of their Vault Registrations deployment. They will discuss some of the difficulties associated with implementing lasting improvements after go-live and how this shaped their change management approach. Then hear how Seagen instilled a continuous improvement model at their organization and what challenges they’ve faced with this cultural shift.

Peter Jons AstraZeneca
Director, Global Regulatory Operations
Verchel Wunpheng Seagen
Senior Manager, Regulatory Information Management

12:00 p.m. - 1:00 p.m.

Veeva shows how the Annual Product Quality Review (APQR) and Quality Management Review (QMR) features in Vault QMS help automate and streamline these time-intensive processes.

Shanul Srivastava Veeva Systems
Solution Consultant

Risk-based approaches are proliferating in clinical trials, including in TMF management. Learn about Veeva’s vision for risk-based and periodic QC in Vault eTMF.

Matthew Carlson Veeva Systems
Product Manager, Vault Clinical Operations

Learn how to incorporate labeling change management into your end-to-end Vault RIM solution.

Christina Howe Veeva Systems
Practice Manager, Vault RIM
Kelly Finlan-Dansbury Veeva Systems
Product Manager, Vault Registrations

See how to streamline adverse event management and eliminate data reconciliation by bringing together clinical, safety, quality, and regulatory applications with Veeva Development Cloud.

Marius Mortensen Veeva Systems
Vice President, Product Management, Vault Safety Suite

Veeva shows how the External Collaboration features in Vault Quality Suite enable seamless and efficient collaboration with partners across multiple processes across Vault Quality Suite.

Chris Boschen Veeva Systems
Senior Product Expert

Hear about the vision for Vault Disclosures, Veeva’s newest application to centralize and simplify global compliance operations.

Matt DeFranco Veeva Systems
Senior Director, Clinical Strategy, Vault Disclosures
Kaitlyn Moore Veeva Systems
Senior Product Manager, Clinical Operations

See how active dossier helps companies maintain a list of current documents for a given product and market.

Abigail Sasdelli Veeva Systems
Team Manager, Vault RIM
Cindy Ling Veeva Systems
Senior Product Manager, Vault RIM Submissions

Learn how the Veeva CDB and Veeva ePRO connection allows for near-real time transfer of patient-entered data for the purpose of reconciliation with other data sources such as EDC and RTSM and the identification of trends and outliers.

Kyle Stephenson Veeva Systems
Director of Product Management, ePRO & eClinRO
Pavel Burmenko Veeva Systems
General Manager, CDB

See how to drive efficiency in your Vault with the latest reporting and dashboards features like Dynamic Distribution Flash Reports.

Pukar Bhandari Veeva Systems
Senior Product Manager, Vault Platform Reports and Dashboards

Sessions
1:00 p.m. - 1:50 p.m.

See the latest advancements in Vault Validation Management, hear what’s next on the roadmap, and get your questions answered by an expert. You’ll learn how to optimize end-to-end validation processes to drive faster, more efficient test execution while maintaining compliance.

Peter Alouche Veeva Systems
Director, Product Management

Explore the diverse array of new GxP training assets that we will be introducing over the next 12 months, learn how we are planning to support more of your organization’s training needs with new vertical libraries, including Corporate Compliance and EH&S, and our other plans to make life easier for you.

Graham O’Keeffe Veeva Systems
General Manager, LearnGxP

Hear Veeva’s vision and roadmap for Vault QMS. Get demos of recent innovations and hear what’s next on the roadmap around topics such as intelligent automation, audits and inspections, and quality risk management (QRM). Also, Veeva’s product experts will answer your questions in this interactive session.

Manaphan Huntrakoon Veeva Systems
Senior Director, Vault Product Management, QMS
Prannoy Kothari Veeva Systems
Senior Product Manager, VPS, QRM, and MedTech Quality

Hear Vault Training’s roadmap and vision, see demos of the latest innovation, and get your questions answered. Highlights will include the enhanced experience for learners, curriculum completion data, and efficient ways to manage your training matrix.

Joby George Veeva Systems
Director, Product Management
Erin Coppola Veeva Systems
Senior Product Manager, Vault Training

Join this interactive session to see demos of the latest advancements in Vault QualityDocs and Vault Station Manager, including External Collaboration for Documents, QR Code Generator, and more. You will also hear what’s next on the roadmap and get your questions answered.

Stephen Chelladurai Veeva Systems
Director, Product Management

Learn how to leverage Vault eTMF features to streamline document QC, including new standard fields. There will also be time to connect with Veeva’s product team for a more in-depth discussion on the future of risk-based QC in Vault eTMF.

Join Seagen for a four-year retrospective value realization journey. They’ll share their maturity growth across Clinical, Regulatory, and Quality enabling structured product and platform management via robust governance and a Veeva center of excellence.

Muralikrishnan Sundararajan Seagen
Executive Director, Business Technology
Karen Kestin Veeva Systems
Global Program Manager

Pharming will share how to streamline daily business interactions across regulatory and IT Roles. They’ll also review pathways and resources for developing RIM expertise and what benefits they’ve seen from their Vault RIM deployment.

Dr. Sadia Chaudhry-Zutshi Pharming Healthcare
Associate Director, Medical Writer

Hear from Syneos Health on how they are increasing efficiency in study delivery through a variety of operational models, and how being a partner with Veeva has enabled them to share key industry trends to support the development of a single workbench environment.

Leonie Christianson Syneos Health
Director, R&D Advisory
Mike McDevitt Syneos Health
Senior VP Biometrics

Hear directly from site professionals and ask questions about their experience maintaining the technology landscape of clinical trials. Hear a range of site perspectives (including a PI, seasoned executive leader, and active study coordinator) as they discuss the role technology plays in building better patient experiences — as well as their challenges, best practices, and advice for sponsors.

Viviënne van de Walle PT&R
PI / CMO
Valrie Patterson University of South Alabama
Clinical Research Nurse
Lauren Wallace Virginia Commonwealth University
Director of Clinical Research Regulatory Affairs
Manny Vazquez Veeva Systems
Director, Vault CDMS Strategy
Bree Burks Veeva Systems
Vice President, Strategy, Site Solutions

Centralizing data is not enough. Centralizing data cleaning and review processes in Veeva CDB unleashes real value. Learn how with CDB’s Review Dashboard, Clean Patient Tracker, Data Provider Access, and other features made for managing data without leaving the cloud.

Eric Jacobson Veeva Systems
Senior Manager, North American Solution Consulting, Clinical Data

Join Vault Safety Suite customers to share best practices, hear from product experts, and discuss latest and upcoming Vault Safety Suite capabilities.

Christina Kim Veeva Systems
Senior Director, Vault Safety
Eric Woolven Veeva Systems
Senior Product Manager, SafetyDocs
Asi Roll Veeva Systems
Director Product Management, Vault Safety

BASE demonstrates the necessary DevOps-integration to establish and build release automation on an enterprise-wide scale. See how to orchestrate large backlogs, configuration synchronization and deployment, testing, and alignment between enterprise projects.

Thomas Videbech BASE life science
Senior Manager
Punit Chordia BASE life science
Senior Practice Engagement Manager

Learn how Sanofi plans to reduce regulatory dossier authoring by half in three years by leveraging lean process, unified data, and advanced technology. They will discuss their automation strategy, milestones on their journey, and their partnership approach with Veeva.

Joseph McLaughlin Sanofi
Head of Business Process & Innovation for Regulatory
Eldar Curovic Veeva Systems
Vice President, Product Management Vault RIM

Tracon will share how they gained efficiencies by integrating multiple technology systems with the Veeva Development Cloud. They’ll also explain how they created a connected clinical landscape to derive greater value from their investment.

Bonne Adams Tracon Pharmaceuticals Inc.
COO

Learn how to streamline data freezing and locking with Vault EDC Snapshot. Identify a specific range of data by custom criteria like subject, status, group or cohort, dates, study events and more — then take action on that data in just clicks. Save time by working in bulk and reusing the Snapshot as data gets updated throughout the study.

Eric Jacobson Veeva Systems
Senior Manager, North American Solution Consulting, Clinical Data

Learn how to effectively validate your multi-vault environment, while simultaneously enhancing operational efficiency and ensuring regulatory compliance. Gilead Sciences and Spotline showcase their collaborative approach, leveraging state-of-the-art processes and technology to make this a reality.

Steve Shimek Spotline
Principal, Life Sciences
Fabio Fernandes Gilead Sciences
Senior Director, Regulatory Systems
Joseph George Veeva Systems
Director Computer Systems Validation Strategy, R&D Services and Quality

Connect
2:00 p.m. - 2:50 p.m.

Learn how Validation Management unifies validation across the Quality Suite, including QualityDocs and QMS to streamline processes and maximize efficiency.

Bernat Rocarols Veeva Systems
Solution Consultant, Quality

Implementing Vault Study Startup is more than just a one-time technology deployment – you also need to align processes, teams, and continuously evolve with new features to maximize your investment. Fortrea will share best practices and key learnings about how they optimized Vault Study Startup across the key pillars of people, process, and technology.

Join Veeva Site Connect customers to share best practices, hear from product experts, and discuss latest and upcoming Site Connect capabilities.

Learn about Vault features that improve the end user experience and don’t require heavy configuration or validation to implement.

Jason Cox Veeva Systems
Manager, Customer Success, Quality & Regulatory
Michael Ferrell Veeva Systems
Product Expert, Vault Platform

Tracking KPIs and cycle times are key to understanding portfolio performance and driving trial efficiencies. Hear which KPIs Vertex measures to identify potential bottlenecks and areas where they can optimize monitoring. Then, engage in roundtable discussions with your peers to discuss top metrics to focus on.

Unified with Vault CTMS and connected with Vault EDC, Vault Payments simplifies payment management and enables companies to pay research sites faster. See how in this group demo.

Ryan Kimble Veeva Systems
Senior Product Manager

Join your regulatory peers for an interactive community meeting with breakout groups for popular topics.

Mary Anne Potok Veeva Systems
Product Expert, Submissions, Archive and Publishing
Lyubena Travaglini Veeva Systems
Product Expert, Vault RIM Registrations

Learn about the innovations and enhancements coming to Veeva ePRO and eClinRO, and ask the Veeva team questions during an interactive Q&A.

Michelle Marlborough Veeva Systems
Senior Vice President, Product Management, Sites & Patients
Kyle Stephenson Veeva Systems
Director of Product Management, ePRO & eClinRO

Five ways to access and export Vault data to support third-party data analytics tools

Mark Arnold Veeva Systems
Director, Product Management, Vault API & SDK

Watch how you can efficiently identify, assess, and mitigate quality risks in Vault QMS for continuous quality improvement.

Prannoy Kothari Veeva Systems
Senior Product Manager, VPS, QRM, and MedTech Quality

In this demonstration, watch how using Vault EDC and Veeva RTSM together allows for a seamless connection between systems, removing the need for duplicate data entry by the site and reducing associated reconciliation efforts for data management teams.

Jennifer England Veeva Systems
Solution Consultant, Veeva RTSM

See how to save time and improve user experience by streamlining multiple workflows into one.

Walid Abou-Chalha Veeva Systems
Senior Product Manager, Vault Platform

Sessions
3:00 p.m. - 3:50 p.m.

See how unified and connected quality risk management can help you improve quality, efficiency, and compliance. See a demo of the latest innovations and engage in live Q&A with the product team.

We’ll review the highlights from the Vault Platform roadmap in a shorter 50 minute session. See how upcoming releases will help organizations improve scalability, user productivity, and operations.

Andy Han Veeva Systems
Vice President Product Management, Vault Platform & Technology
Michael Ferrell Veeva Systems
Product Expert, Vault Platform

Learn how Veeva is bringing innovation to RTSM. Hear about our overall strategic vision and roadmap for this mission critical product and ask the Veeva RTSM leadership team questions during an interactive Q&A.

Lee Gamble Veeva Systems
Director, Product Management Veeva RTSM
Steve Simmerman Veeva Systems
General Manager, Veeva RTSM

Learn the ways in which customers use Vault Quality Suite to collaborate with external business partners to streamline processes and maximize efficiency.

Hear best practices for using product reference data in Vault Quality Suite, and join a roundtable discussion on customer scenarios and requirements. This session is best suited for IT and System Owners in top biopharma companies.

Learn how you can manage and conduct GxP and non-GxP training in a single LMS. This session will explore the definitions of GxP and non-GxP, and share best practices for configuration and reporting.

Learn how Veeva ePRO and Veeva eClinRO simplify the design, management, and completion of electronic patient-reported and clinician-reported outcomes.

Andrew Rohrbaugh Veeva Systems
General Manager, ePRO & eClinRO
Michelle Marlborough Veeva Systems
Senior Vice President, Product Management, Sites & Patients
Kyle Stephenson Veeva Systems
Director of Product Management, ePRO & eClinRO

Learn about high impact reporting capabilities, and how to leverage them for high-value reporting use cases in Vault QMS.

Learn how Atara tests and validates new functionality with each Veeva release cycle. They’ll also share strategies for streamlining some key steps in the process for more efficient technical operations.

Matt Neal Atara Biotherapeutics
Senior Director, Global Regulatory & Quality
Joseph George Veeva Systems
Director Computer Systems Validation Strategy, R&D Services and Quality

See how Sandbox Snapshots enable users to save configurations and data for repeatable testing and faster refreshes.

Kunal Morparia Veeva Systems
Senior Product Manager, Vault Platform