Outsourcing Clinical Trials with Better Oversight, Efficiency, and Speed

Gain efficiency with real-time data access.

Better Trial Efficiency with the Right Partners

“When sponsor and CRO partnerships are developed with clear processes, expectations, and proactive training, we can design execution and oversight for quality and efficiency.”

Regina Norelli

Executive Director, Clinical Data and Sample Management, Replimune

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Your Data, Your Decision: Requesting the Right Clinical Platform from Your CRO

Sid Mohamoodally, Senior Director, CRO Strategy

Step 1

During the RFI

Inquire about the clinical data and operations landscape of the CRO to ensure systems are fit-for-purpose.

Step 2

During the RFP

Ask about specific experience with Veeva. If the CRO does not have Veeva experience, make them aware of your preference, the benefits of using Veeva, and ability to train their teams.

Step 3

During bid defense

Ask for past examples of how the CRO has delivered similar studies, lessons learned, comparisons, and how they can be applied to the study being bid on.

6 changes you need to know, including risk-based oversight

Veeva DQS

Biopharma eliminates 90% of SAS listings

Enhancing Site and Patient Experience

Veeva EDC

Support site satisfaction with quality data entry from the point of entry

VeevaID and Veeva EDC

Fortrea eliminates 100% of login support calls

Veeva EDC and Veeva DQS

Replimune reduces data entry by 30% for sites

Simplify End-to-End Data Flow with Productized Connections

See the clinical trial data flow showing product connections between Veeva EDC, Veeva DQS, Veeva RTSM, and Veeva eCOA.

Learn how Inhibrix eliminated redundant processes.

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Clinical Operations – EDC

Eliminate transcription errors, duplicate data entry, and separate logins.

Safety – EDC

Automate clinical serious adverse events (SAE) reporting to safety, increase quality of PV data, and reduce reconciliation.

RTSM – Clinical Operations

Rely on Clinical Operations to be your single source of truth for core study data across Veeva Applications.

eCOA – Clinical Operations

Streamline study start up and close out procedures with study and eCOA data alignment.

RTSM – DQS

Speed aggregation and cleaning of patient data by connecting RTSM with DQS.

RTSM – EDC

Simplify subject and randomization data management.

CRO Partners

Find your CRO Accredited Partner

CROs providing best-in-class services across unified clinical products.

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CROs Strengthening Sponsor Collaboration with Veeva

“Sponsors have overall oversight of the entire study, so it’s clearer and easier for us to communicate what the metrics look like, especially when you have studies with a high volume of data and very fast timelines.”

Principal Clinical Data Scientist

Global CRO

“It has given transparency and a higher level of trust because they see exactly what’s going on at the site. It has made our weekly meetings more effective because we don’t only talk about the classic updates, but also where there’s risk.”

Staci McDonald

Vice President of Global Clinical Operations, Celerion

“Veeva and IQVIA are very aligned on the future – how AI comes into place and how we can support our sponsors together.”

Sandra Martin

Director Clinical Data Management, IQVIA

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“We are no longer cleaning data in silos, one side EDC, one side external data, but now we have one big interface where we are cleaning the entire data set.”

Bireshwar Saha

Head of Global Programming and Analytics, Fortrea

“The way Veeva Clinical Data and the whole Vault platform fits together drives level of performance improvement in data management by anticipating and enabling data managers to do what they need to do.”

Dr. Nicholas Lakin

Senior Managing Director, Syneos Health Consulting