Registration is Now Open
Join us at Veeva R&D Summit, North America on September 8-10, 2019 at the Pennsylvania Convention Center to hear the latest news and market trends in the industry, experience innovative technology, and share best practices.
Veeva R&D Summit is an annual gathering of pharma, biotech, and medical device and diagnostics leaders in clinical, regulatory, quality, and IT.
Last year, over 1,400 life sciences leaders and experts gathered at Veeva Global R&D Summit to hear from BMS, Cara Therapeutics, Janssen, and more. With more than 65 breakout sessions featuring customer case studies in clinical operations, clinical data management, regulatory, quality, and IT this year will be our most exciting event yet.
The conference is complimentary to Veeva customers and invited guests. Space is limited – register now.
Key topics will include:
Clinical Operations
- Transforming end-to-end clinical trial processes with a unified clinical operations suite.
- Enhancing collaboration and data sharing between sponsors, CROs, and investigator sites.
- Improving trial efficiency, quality, and oversight.
- Enabling active TMF operating models within a unified clinical environment.
Clinical Data
- Speeding study timelines, including study builds and database locks.
- Transforming UAT processes with a risk-based approach and live updates.
- Adopting an agile design methodology with collaborative, spec-less design.
- Modernizing the clinical data experience for sites, sponsors, and CROs.
Regulatory
- Unifying submission development from planning through publishing.
- Simplifying variation management and tracking approval status.
- Aligning headquarters and affiliates to optimize regulatory processes.
- Maximizing Vault RIM value with implementation insights.
Quality and Manufacturing
- Quality management best practices.
- Practical recommendations for audit and inspection readiness.
- Guidelines for deploying a training solution in a unified quality suite.
- Opportunities for modernizing quality management including quality risk management.
Drug Safety
- Streamlining adverse event collection, evaluation, and reporting.
- Enabling collaboration with real-time oversight.
- Ensuring quality, compliance, and completeness of safety information.
- Staying current on regulatory changes.
Veeva Vault Platform
- Extending Vault with Vault Objects and SDK.
- Data management strategy across Vaults.
- Vault security best practices.
- Gaining insight with reporting and dashboards.
Meet great people, learn new things
Join more than 1,600 life science professionals at this year’s Summit to connect and learn within this powerful community. Summit will offer a number of great ways to connect with your industry peers, including:
Community lounges were open during the event for networking with your colleagues.
Attendees discussed common areas of interest over breakfast and lunch.
Summit Attendees
Here is a snapshot of companies who attended last year’s conference.
