
ABOUT VEEVA SYSTEMS, INC.
Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves. For more information, visit veeva.com.
CONTACT INFORMATION
Veeva Systems, Inc.
4280 Hacienda Drive
Pleasanton, CA 94588
UNITED STATES
Phone: 925 452 6500
Fax: 925 452 6504
FEATURED ARTICLES
- There Is More To CDMS Than EDC
- Using Agile Design To Accelerate R&D
- Integrating EDC And RTSM Solutions
- Clinical Trials: Are We Any Closer To Solving The Rubik’s Cube?
- State Of Digital Clinical Trials: How Clean Is Your Data?
- State Of Digital Clinical Trials: Will Traditional EDC Exist Ten Years From Now?
- What Should be In Your Digital Trial Toolkit?
- The Future Of Digital Trials: On The Floor At DIA
- Adopting Vault CDMS Accomplishments And Lessons Learned
- State Of Digital Clinical Trials Podcast: Life Sciences In Europe And Breaking Down The Barriers
- New Industry Regulations: Three Implications For TMF
- 3 Ways To Future-Proof Digital Clinical Trials
- Building A Digital Foundation For Patient-Centric Trials
- Site Engagement Considerations When Adopting Study Start-Up Technology
- Top 3 Tips To Better Work With Sites
- Top 3 Criteria To Select A Study Start-Up Application
- The Importance Of Improving Study Start-Up Timelines
- Accelerating Digital Platform Adoption
- Exchanging Regulatory Packages With Sites
- Vanderbilt’s Advice For Sponsors: How To Make Working With Your EDC Easier For Sites
- Vault CTMS For Insourced And Outsourced Trial Management
- Improving Sponsor-CRO Collaboration And Oversight
- Fireside Chat With Moderna
- Preparing For Virtual Inspections And Ongoing Regulatory Changes
- Alexion: Building A Multi-Year TMF Strategy
- Takeda: Driving Efficiencies With Focus On Quality
- Digitizing Clinical Trials – Strategies To Support Patients, Sites, And Sponsors
- A Digital Future: Evolving Beyond Decentralized Trials
- Vault CTMS Oversight Deep Dive
- Vault CTMS Risk-Based Study Management
- LEO Pharma: Faster Trials And A Better Patient Experience
- How One Top 20 Pharma Is Driving Operational Process Improvements Through Digital Transformation
- Leveraging eConsent To Benefit Sites And Patients
- Illumina Cuts 5 Months From Study Builds And Eliminates Regression Testing
- Is It Worth The Effort To Switch To Veeva's EDC?
- Veeva eConsent: Improved Patient Experience With End-To-End Informed Consent
- Advancing Site Payments: A Win-Win For All
- Achieving A Next-Generation Clinical Environment
- Simplify And Streamline Study Builds
- Lotus Clinical Research Speeds Study Startup By 67% With Veeva Clinical Suite
- MHRA Identifies Common Flaw In Managing Protocol Deviations
- CROs Pave The Way For Digital Clinical Trials
- Global Device Company Takes Holistic Approach To Clinical Operations And Data Management
- Streamlining Clinical Study Design: Lessons Learned From The Pandemic
- The Industry’s Move Toward Digitally Connected Clinical Trials
- Automate Information Sharing With Veeva Site Connect
- GSK Puts Data First In New Clinical Agility Benchmarks
- Digital Clinical Trials Survey Report
- Rethinking Clinical Trials For The Future
- Improve Data Quality, Reduce Operational Risk, And Allocate Resources More Effectively
This website uses cookies to ensure you get the best experience on our website. Learn more