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AUSTIN, Texas and BARCELONA, Spain, Dec. 14, 2022 /PRNewswire/ -- Veeva Systems (NYSE: VEEV) and CDISC are pleased to announce that Dan Crawford, Principal Consultant for Veeva Clinical Database (CDB), has been elected Chairman of the CDISC Advisory Council (CAC). The CAC is made up of representatives of CDISC Platinum members who play an important role in shaping the development and direction of CDISC, providing the CDISC executive team with recommendations that support CDISC goals.

A longtime CDISC volunteer, Dan is an expert on CDISC standards and has been instrumental in the development of the CDISC data collection standard, CDASH. As CAC chair, he will work closely with clinical leaders from top 20 pharmaceuticals, emerging biotechs, clinical research organizations (CROs), and technology providers. Dan will also serve as an advisor to the CDISC Board of Directors to represent the opinions, perspectives and interests of the CAC.

"I am honored to have been elected chair of the CDISC Advisory Council and to be the voice of its representatives," Crawford explained. "Veeva is on the front lines working with customers to transform data collection and cleansing and help data stewards spend more time on valuable scientific analysis. I look forward to bringing my experience developing and implementing CDISC standards forward industry and communicate the benefits of data standards.

With the adoption of CDISC standards, life sciences companies can start and close trials and more quickly deliver normalized data to regulatory agencies. This can speed up the execution of studies and access to new medicines and treatments.

"The CAC is essential to ensure that CDISC standards continue to drive operational efficiencies in the organizations that use them to expedite the regulatory review process and reduce time to market," said David A. Evans, CDISC President and CEO. . We are delighted to welcome Dan and his experience as CAC chair."

Veeva is proud to support life sciences companies with Veeva Vault CDMS, a unified data management solution for the capture, cleansing, and encryption of clinical data. For more information, visit the Vault CDMS web page.

Additional InformationTo learn more about Veeva Vault CDMS, visit: veeva.com/eu/CDMS Connect with Veeva on LinkedIn: linkedin.com/company/veeva-systems

ABOUT CDISCCDISC brings clarity to clinical research by bringing together a global community to develop and promote the highest quality data standards. CDISC standards, required by the US Food and Drug Administration (FDA) and Japan Pharmaceuticals and Medical Devices Agency (PMDA), recommended by the China National Medical Products Administration (NMPA) and adopted by the world's leading research organizations enable accessibility, interoperability and reuse of data. With the help of the CDISC standards, the entire research community can maximize the value of data for more efficient and meaningful research that has an inestimable impact on global health. CDISC is a 501(c)(3) global non-profit charitable organization headquartered in Austin, Texas with hundreds of employees, volunteers and member organizations around the world. Learn more on the website www.cdisc.org.

About Veeva Systems Veeva is the world leader in cloud software for the life sciences industry. Committed to innovation, product excellence and customer success, Veeva serves more than 1,000 customers, from the world's largest pharmaceutical companies to emerging biotech companies. 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 the website veeva.com/eu.

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