Watch Sessions On Demand
Veeva Summit Connect is over but the learning and exchange of ideas doesn't have to stop here. Missed a session or want to watch it again? Head over to the content directory below and find a topic you want to learn more about. Contact our team with any questions on product roadmaps and for more information.
Keynote Replays
Opening Keynote
Digital Innovations Streamlining Drug Development
GSK
Top Trends in Global Supply Chains
Session Replays
GSK discusses achievements and lessons learned from transforming TMF operations. They outline the steps they are now taking to achieve best-in-class TMF management and inspection readiness.
Digitization across clinical operations is accelerating as the industry embraces more streamlined trial management and patient-centric approaches to study execution. Hear industry leaders from Roche and TFS discuss how these new models are reshaping and transforming the industry.
Watch this session and see how Vault Clinical Operations applications work together in a unified suite for end-to-end trial management.
MyVeeva for Patients is a new application that makes it easier to deliver a paperless, patient-centric clinical trial. Learn how MyVeeva will enable a better patient experience and speed study conduct.
Our services experts will share Vault CTMS tips and tricks - and lessons learned - to make site monitoring more efficient and easier for CRAs and reviewers in this session.
Discuss with your peers how to prepare for and facilitate digital inspections - especially relevant for sponsors that outsource their clinical trials.
Learn about the EMA's Clinical Trial Regulation and how Veeva Vault can help you manage this new process.
Hear how KCR, a digital CRO, ensures transparency, digital inspection readiness, and predictive analytics for their sponsors by leveraging Vault applications.
Hear best practices using Vault clinical reports to get the visibility you need to your trial data in this advanced session for emerging biopharma and CROs.
Bayer will share their lessons learned from the pandemic and approach to study start-up optimization, implementation best practices, and deployment strategies to boost end-user adoption.
Get an in-depth look at how TMF Transfer solves inspection readiness needs and hear how Nestlé uses it to work more effectively with CRO partners.
Learn how GSK intends to bridge the information gap between clinical and regulatory teams with the Vault Clinical Operations to RIM Connection. They'll review how they planned, configured, and evaluated this connection with the goal to drive greater alignment, consistency, and speed.
See how to navigate cross-functional business processes with the Veeva Development Cloud. We’ll demonstrate several use cases that touch clinical, quality, regulatory, and safety.
Data management faces challenges: from the complexities of trial design to an increase in data sources. The global head of clinical data management at Sanofi shares his predictions and goals for the next decade.
Supplemental materials:
Blog: Sanofi Designing a Data Management Strategy for the Future
Learn efficient strategies for initial system validation. Bioforum and Veeva cover best practices for managing new releases and the resources available to support system validation.
Supplemental materials:
Demo: Vault CDMS Targeted SDV
COVID exposed inefficiencies in the traditional way of doing business. Hear how CROs partner with Veeva to identify new ways of working and bringing speed and agility to clinical processes.
Supplemental materials:
PR: How Sponsors and CROs Benefit from the Veeva Vault CDMS Partner Program
Veeva is developing a reliable and repeatable way to migrate in-process clinical trials from legacy EDC systems to Vault CDMS. Hear case studies on migrations and the automation and planning behind their success.
See how to navigate cross-functional business processes with the Veeva Development Cloud. We’ll demonstrate several use cases that touch clinical, quality, regulatory, and safety.
See how Alvotech ensures functional job readiness by capturing on-the-job training evaluation as part of a curriculum with Vault Training.
Argenx and Epista will share best practices and lessons learned in implementing Vault QualityDocs and Vault QMS to streamline quality processes across the enterprise.
A top 20 pharma shares their quality transformation journey to increase agility, transparency, and partner collaboration, bringing drugs to patients faster.
Hear the outcome of FDA-sponsored St.Gallen’s quality metrics and operational excellence research highlighting the importance of quality metrics in driving continuous improvement.
Watch GSK and UCB in this panel discussion on externalization trends and addressing their impact on the effectiveness of quality management systems. We will also discuss how Vault Quality streamlines external collaboration, highlighting specific use cases.
Quality and regulatory teams handle thousands of post-approval changes every year. Watch this session to hear how UCB will effectively manage these changes, reduce manual steps, and speed delivery with Veeva’s unified platform.
See how to navigate cross-functional business processes with the Veeva Development Cloud. We’ll demonstrate several use cases that touch clinical, quality, regulatory, and safety.
IDMP is more than just a regulation. It's an opportunity to improve business process efficiency across the entire organization. Watch this panel to hear how AstraZeneca, Bristol Myers Squibb, and Takeda are using IDMP preparation to re-think their unified RIM strategy.
Supplemental materials:
Read Article
For companies that manage post-patent medicines, it can be challenging to incorporate new acquisitions into their existing portfolio. Hear how Pharmanovia implemented a unified platform to help them seamlessly transition new medicines and optimize regulatory operations.
Tracking contractual obligations is a crucial process for regulatory affairs teams. Watch this session to hear how Bayer AG is leveraging Vault RIM to improve global transparency into contractual obligations while maintaining compliance.
With the rapid evolution of technology, organizations are adapting to system updates every few months rather than every few years. Join this panel to hear how IBSA, UCB, and NNIT are tackling change management to optimize business outcomes.
Supplemental materials:
Read Article
Learn about the EMA's Clinical Trial Regulation and how Veeva Vault can help you manage this new process.
Learn how GSK intends to bridge the information gap between clinical and regulatory teams with the Vault Clinical Operations to RIM Connection. They'll review how they planned, configured, and evaluated this connection with the goal to drive greater alignment, consistency, and speed.
Quality and regulatory teams handle thousands of post-approval changes every year. Watch this session to hear how UCB will effectively manage these changes, reduce manual steps, and speed delivery with Veeva’s unified platform.
See how to navigate cross-functional business processes with the Veeva Development Cloud. We’ll demonstrate several use cases that touch clinical, quality, regulatory, and safety.
How do you ensure that your team is getting the full benefit of a new RIM solution? Join this panel to understand how GE Healthcare, Mundipharma, and Recordati are tracking process maturity, evaluating improvements, and making changes to better realize their Vault RIM investment.
BMS centralizes pharmacovigilance document management with Vault SafetyDocs to streamline collaboration and enable an always inspection ready PSMF. Hear how they are providing global visibility and automatically generating a current and region-specific PSMF – at any time, easily staying compliant with local regulatory requirements.
Hear Vault Safety implementation experiences and impact of a unified solution on safety processes. We’ll examine industry trends and discuss technology’s role in pharmacovigilance.
See how to navigate cross-functional business processes with the Veeva Development Cloud. We’ll demonstrate several use cases that touch clinical, quality, regulatory, and safety.
Get an overview on approaches, key considerations, and best practices for implementing the Vault Safety Suite of products. We’ll explore the unified and connected pharmacovigilance solution and how to enable end-to-end safety processes.
AstraZeneca is on a journey to transform end-to-end drug development with digital processes, enhanced data, and artificial intelligence. Watch this session to learn about their vision, lessons learned, and the benefits of seamless information flow from clinical trial design through post-marketing surveillance.
Learn how GSK intends to bridge the information gap between clinical and regulatory teams with the Vault Clinical Operations to RIM Connection. They'll review how they planned, configured, and evaluated this connection with the goal to drive greater alignment, consistency, and speed.
Quality and regulatory teams handle thousands of post-approval changes every year. Watch this session to hear how UCB will effectively manage these changes, reduce manual steps, and speed delivery with Veeva's unified platform.
See how to navigate cross-functional business processes with the Veeva Development Cloud. We’ll demonstrate several use cases that touch clinical, quality, regulatory, and safety.
Hear how GSK is designing an organizational operational model to align with the Veeva Development Cloud. They’ll explain how they’re shifting from siloed teams to a center of excellence in 2023 and what challenges they expect along the way.
AstraZeneca is on a journey to transform end-to-end drug development with digital processes, enhanced data, and artificial intelligence. Watch this session to learn about their vision, lessons learned, and the benefits of seamless information flow from clinical trial design through post-marketing surveillance.
Learn how GSK intends to bridge the information gap between clinical and regulatory teams with the Vault Clinical Operations to RIM Connection. They'll review how they planned, configured, and evaluated this connection with the goal to drive greater alignment, consistency, and speed.
Quality and regulatory teams handle thousands of post-approval changes every year. Watch this session to hear how UCB will effectively manage these changes, reduce manual steps, and speed delivery with Veeva's unified platform.
See how to navigate cross-functional business processes with the Veeva Development Cloud. We’ll demonstrate several use cases that touch clinical, quality, regulatory, and safety.
Hear how GSK is designing an organizational operational model to align with the Veeva Development Cloud. They’ll explain how they’re shifting from siloed teams to a center of excellence in 2023 and what challenges they expect along the way.