Veeva Clinical Platform | Veeva
Veeva Clinical Platform
Simplify and Standardize Clinical Trials
Better efficiency and experience for sponsors, sites, and patients
Announcing Veeva eSource to Eliminate Paper and Streamline Data Flow
Veeva Clinical Platform
Run studies faster with a complete, high quality platform
Reduce effort and connect with sponsors on a standard platform
Keep patients connected through one application
Products
Connected Products in a Complete Clinical Platform
Clinical Operations
Unify clinical systems and processes on a single cloud platform to enable end-to-end trial management.
[**Veeva eTMF**
Ensure TMF quality, timeliness, and completeness.](/content/products/veeva-etmf/index.html)
[**Veeva CTMS**
Optimize trial management and monitoring for all studies.](/content/products/veeva-ctms/index.html)
[**Veeva Payments**
Streamline payments to clinical research sites.](/content/products/veeva-payments/index.html)
[**Veeva Study Startup**
Simplify site selection and speed study start-up.](/content/products/veeva-study-startup/index.html)
[**Veeva Site Connect**
Automate document exchange during start-up, execution, and closeout.](/content/products/veeva-site-connect/index.html)
[**Veeva Study Training**
Manage GCP and study-specific training.](/content/products/veeva-study-training/index.html)
[**Veeva Disclosures**
Share registrations and results disclosures with registries.](/content/products/veeva-disclosures/index.html)
[**Veeva OpenData Clinical**
Global reference data of sites, investigators, and their affiliations.](/content/products/opendata-clinical/index.html)
Veeva Clinical Operations Connections
Clinical Data
Accelerate study timelines with modern applications.
[**Veeva EDC**
Collect, clean, and review study data.](/content/products/veeva-edc/index.html)
[**Veeva DQS**
Aggregate, clean, and transform clinical data from multiple sources.](/content/products/veeva-dqs/index.html)
Veeva Clinical Data Connections
Veeva RTSM
Enterprise standard solution for all trial types.
Veeva eCOA
Simplify the design, management, and completion of eCOA.
Clinical Research Sites
Simplify the site experience.
[**Veeva SiteVault**
A free eISF for research sites to digitize study binders, enable remote monitoring, and collaborate with sponsors.](https://sites.veeva.com/)
[**VeevaID**
Single sign-on for clinical researchers across all sponsor systems.](/content/resources/veeva-introduces-study-portal-and-veevaid-to-streamline-research-site-trial-execution/index.html)
Patients
Make trial participation more accessible and convenient.
[**MyVeeva for Patients**
Keep patients informed and connected with a single application for all their trial activities.](/content/products/patient-experience/index.html)
“We prioritized the modernization and simplification of our clinical trial ecosystem.”
Bryan Kropp
AVP, head of clinical data management and standards at Merck
“Collaboration between data management and clinical operations has always been important, but it was never truly supported by technology. Now, we have a platform that facilitates that collaboration.”
Michael Haushalter
Senior Principal Capability Manager, Boehringer Ingelheim
“Research sites are focused on patient care, so alleviating administrative burden is not a luxury but a necessity. Veeva is delivering on the vision of offering solutions that are centric to the needs of sites.”
Dr. Vivienne van de Walle
Principle investigator, medical director, PT&R
“When you bring technology and innovation together with people and processes…you get back to our key objective, which is bringing medicines to patients faster.”
Penny Carlson
VP Head of Innovation and Data, Takeda
“Our effort to connect the study across different applications has gone from three months to five minutes.”