Vital Therapies Readies Clinical & Regulatory Operations with End-to-End Regulated Content Management Solution in the Cloud from Veeva Systems

Biotech turns to Veeva Vault to drive efficiency from study start-up to submissions

PLEASANTON, Calif.--()--With an investigational combination biological product in Phase III clinical trials and a recent IPO, Vital Therapies, Inc. is readying its clinical and regulatory operations for global collaboration and greater efficiency with cloud-based Veeva Vault eTMF and Veeva Vault Submissions content management applications from Veeva Systems. Together, the new Vault applications allow Vital Therapies to align document workstreams from study start-up through to submissions. The company is now rolling out Vault as it prepares for its potential first Biologics License Application (BLA) filing.

Veeva Vault – easily and securely accessible in the cloud – enables efficient collaboration between Vital Therapies’ external partners, internal teams across clinical and regulatory, and study sites globally. “We wanted an end-to-end solution that would allow improved efficiency, enable streamlined operations, and provide team members with access to product and study documentation in a structured and secure location. With Veeva Vault, it’s easier to share information,” said Heidi Spanish, director of global regulatory and quality operations for Vital Therapies. “Veeva Vault will also scale to grow with our organization as we drive toward our goal of commercialization.”

Vital Therapies noted the synergy it gains from leveraging a single system for regulated documents. “Veeva Vault connects workstreams between clinical and regulatory, which improves productivity. Users no longer have to pull documents from multiple places,” added Spanish. “And, we no longer need multiple versions of the same document. We now have one version – with content structured largely based on the DIA TMF Reference Model – accessible to teams globally. We used to spend hours comparing different versions, but Veeva Vault saves us time and prevents errors by providing document version control. Vault also reduces time spent searching or chasing down documents when preparing submissions.”

As a growing organization, Vital Therapies wanted to minimize the infrastructure and operational investments that traditional on-premise systems require, and focus its resources on research and development instead. “The cloud is a good way for growing companies to implement advanced business applications like Veeva Vault. System maintenance is provided by Veeva with the option to make changes ourselves or through Veeva’s services. The upgrades to Vault are available regularly, allowing us to enable them as needed for easy access to the latest innovations from Veeva,” added Spanish.

Vault eTMF and Vault Submissions are part of Veeva Vault, a cloud-based suite of integrated content management applications and platform for the life sciences industry. Vault spans clinical, quality, commercial, and medical – every major part of a life sciences company – giving pharmaceutical, biotechnology, and medical device companies the ability to deploy a single content management system globally. Helping companies connect securely in the life sciences cloud, Vault provides complete control from start to finish, as well as the easy accessibility, visibility, and agility needed to speed time to market. All Vault applications offer real-time reporting and dashboards; an intuitive, consumer-web interface; and a true multitenant cloud architecture that continuously delivers rapid innovation.

“The people at Veeva have worked in pharma so they understand our requests and provide good advice. It has been a great experience,” concluded Spanish.

Additional Information

About Veeva Systems

Veeva Systems Inc. (NYSE:VEEV) is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 200 customers, ranging from the world's largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices in Europe, Asia, and Latin America. For more information, visit www.veeva.com.

Forward-looking Statements

This release contains forward-looking statements, including statements regarding benefits from the use of Veeva’s solutions, demand for Veeva’s solutions, and general business conditions. Any forward-looking statements contained in this press release are based upon Veeva’s historical performance and its current plans, estimates and expectations and are not a representation that such plans, estimates, or expectations will be achieved. These forward-looking statements represent Veeva's expectations as of the date of this press announcement. Subsequent events may cause these expectations to change, and Veeva disclaims any obligation to update the forward-looking statements in the future. These forward-looking statements are subject to known and unknown risks and uncertainties that may cause actual results to differ materially. Additional risks and uncertainties that could affect Veeva’s financial results are included under the captions “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations,” in the company’s filing on Form 10-Q for the period ended July 31, 2014, which is available on the company’s website at www.veeva.com under the Investors section and on the SEC’s website at www.sec.gov. Further information on potential risks that could affect actual results will be included in other filings Veeva makes with the SEC from time to time.

Contacts

Veeva Systems Inc.
Lisa Barbadora
Public Relations
610-420-3413
pr@veeva.com

Release Summary

Vital Therapies Readies Clinical & Regulatory Operations with End-to-End Regulated Content Management Solution in the Cloud from Veeva Systems

Contacts

Veeva Systems Inc.
Lisa Barbadora
Public Relations
610-420-3413
pr@veeva.com