## Veeva EDC

# The Most Connected and Innovative EDC

Electronic Data Capture (EDC) provides an end-to-end environment to collect, review, and process site-reported patient trial data.

During study start, EDC is used to design participant Case Report Forms and quality control checks.

During study execution, EDC collects all patient form data, local labs, and medical coding. Quality controls include querying, targeted source data verification (SDV) and protocol deviations.

During study close, EDC provides data lock and post-processing features, including automatic end-of-study media creation and archiving.

###### Announced 2016 Status Mature Customers 100+

Download Product Sheet](/content/wp-content/uploads/2023/07/Veeva-Product-Sheet-Vault-Clinical-Data.pdf?1/index.html)

[**Introducing Veeva Study Builder Agent to configure studies in as little as one day**](/content/resources/new-veeva-study-builder-agent-to-configure-clinical-studies-in-as-little-as-one-day/index.html)

###### Impact

### Proven value for complex studies

### 50%
faster study builds

### 100%
elimination of known custom functions

### 9x
faster to implement study changes

###### Why Veeva EDC

### Modern EDC for agility and efficiency

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#### Build studies faster

Design complex studies with an in-product specification studio built on Agile Design principles.

#### Get cleaner data with less effort

Speed SDV and medical assessments with role-based user interfaces that prompt action.

#### Run complex trials with no downtime

Flexibly design and operate all studies, including master protocols and adaptive designs.

#### Connect clinical teams

Leverage [Veeva Connections](/content/products/vault-platform/veeva-connections/index.html) to share data and collaborate across your entire study team.

###### Customer Success

### Eight of the Top 20 biopharmas switched to Veeva EDC

“We see up to 50% faster build times with

Veeva CDMS.”

##### Leonie Christianson, Business Lead, Veeva CDMS Project

###### GSK

[Read case study](/content/customer-stories/adopting-vault-cdms-accomplishments-and-lessons-learned/index.html)

“We completed three rounds of UAT in two days.”

##### Michelle Harrison, Associate Director, Clinical Data Management

###### Vertex Pharma

[Discover agile study builds](/content/vertex/index.html)

“Having a complex trial design doesn’t mean you need to have a complex build.”

##### Tanya du Plessis, VP of Data Strategies and Solutions

###### Bioforum

[Read case study](/content/customer-stories/how-vault-cdms-improves-the-speed-and-quality-of-bioforums-study-builds/index.html)

###### Resources

### Explore and Learn

[**Read Features Brief**  **Veeva EDC Features Brief**\
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 [**Read Blog**  **A Business Case to Standardize EDC Across Study Phases**\
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 [**Read White Paper**  **Eliminate Custom Functions with Veeva EDC**\
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 [**Learn More**  **Why Eight Top 20 Biopharmas Switched their EDC**\
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 [**Learn More**  **Meet the Sponsors and CROs Succeeding with Veeva EDC**\
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 [**Veeva EDC Demo Hub**  **See Veeva EDC in Action**\
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### Interested in learning more?

[Contact Us](/content/contact-us/index.html) [Download Product Sheet](/content/wp-content/uploads/2023/07/Veeva-Product-Sheet-Vault-Clinical-Data.pdf?1/index.html)