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Veeva Announces New Application to Speed Validation ExecutionVeeva Vault Validation Management to streamline end-to-end validation processes for audit readiness and compliance BARCELONA, Spain, Sept. 15, 2021 /PRNewswire/ -- Veeva Systems (NYSE: VEEV) today announced Veeva Vault Validation Management, a new application that will enable more efficient, cost-effective validation lifecycle management. Life sciences companies will be able to create and organize validation activities, manage a global library of test scripts, and execute and record validation data electronically for faster test execution and greater compliance. "Manual validation processes are ineffective, draining resources and increasing operational cost," said Mike Jovanis, vice president of Veeva Vault Quality. "Veeva Vault Validation Management will allow customers to optimize the end-to-end validation lifecycle with paperless execution for increased efficiency and audit readiness." Vault Validation Management will reduce manual processes and eliminate silos for better tracking and alignment across validation activities and projects. Quality teams will be able to use suggested artifacts and templates to drive consistency, ensuring good documentation practices (GDP) and data integrity. Seamless integration with Veeva Vault QualityDocs and Veeva Vault QMS will connect key artifacts, discrepancies, and change controls, improving transparency and data accessibility. Intuitive dashboards also display critical metrics like status and cycle times for better traceability across validation projects. Vault Validation Management is part of the Veeva Vault Quality Suite, including Vault QMS, Vault QualityDocs, Veeva Vault Training, Veeva LearnGxP, Veeva Vault Station Manager, and Veeva Vault Product Surveillance to automate and harmonize quality processes globally. Vault Quality Suite enables companies to easily manage quality in one unified solution and delivers the power and scalability needed across the life sciences value chain. Vault Validation Management is planned for availability in the second half of 2022. To learn more about Vault Validation Management, visit veeva.com/eu/VaultValidationManagement. Attend Veeva R&D and Quality Summit Connect on 14 October 2021 to hear more about the new offering, Merck & Co., Inc.'s digital quality transformation journey, and Supernus Pharmaceuticals' organizational change management best practices for quality modernization. The online event is open to life sciences industry professionals. Register and stay up to date on program details at veeva.com/Summit. Additional Information About Veeva Systems Forward-looking Statements
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