Vault Quality en Vault RIM-toepassingen automatiseren workflows voor volledig inzicht in verandering controleprocessen en snellere productontwikkeling
BARCELONA, Spanje– (BUSINESS WIRE) – Veeva Systems (NYSE: VEEV) heeft vandaag aangekondigd dat Epredia, een wereldleider op het gebied van precisiekanker en weefseldiagnostiek, de toepassingen Veeva Vault Quality en Veeva Vault RIM overneemt om de controle over veranderingen tussen kwaliteitsmanagement en regelgeving te automatiseren operaties. Veeva MedTech-oplossingen brengen kwaliteits- en regelgevingsinformatie samen op één platform voor meer transparantie tussen processen en naleving van veranderende regelgeving. Nu kan Epredia het beheer van wijzigingen verenigen om de samenwerking te versterken en de productlevenscyclus te versnellen.
Epredia Adopts Veeva MedTech Solutions to Unify Change Control Across Quality and Regulatory
Vault Quality and Vault RIM applications automate workflows for full visibility into change control processes and faster product development
BARCELONA, Spain–(BUSINESS WIRE)– Veeva Systems (NYSE: VEEV) today announced that Epredia, a global leader in precision cancer and tissue diagnostics, is adopting Veeva Vault Quality and Veeva Vault RIM applications to automate change control between quality management and regulatory operations. Veeva MedTech solutions bring together quality and regulatory information on one platform for better transparency across processes and compliance with changing regulations. Now Epredia can unify change control to strengthen collaboration and speed the product lifecycle.
“Veeva MedTech solutions harmonize our global quality assurance and regulatory affairs processes with a single source of content and data,” said Mark Ramser, senior director of global quality at Epredia. “With complete visibility throughout our change management processes, we can make more informed decisions and get products to market much faster.”
Vault Quality and Vault RIM seamlessly connect change control processes to reduce manual overhead and minimize risk of errors. Changes to approved products, manufacturers, and suppliers are managed from end-to-end to better meet diagnostic reporting and visibility requirements, including 21 CFR part 820, ISO13485, and IVDR. Vault Quality handles change control strategies, decisions, and quality document management, while Vault RIM streamlines decision and impact analysis, submission planning and tracking, and document authoring and archiving.
“There is a significant opportunity for MedTech companies to improve how teams across functions work together,” said Jim Diefenbach, general manager of Veeva MedTech. “Epredia is modernizing quality and regulatory processes to simplify the end-to-end workflow for managing product changes and accelerate the total product lifecycle.”
Epredia is adopting regulatory applications Vault Submissions and Vault Submissions Archive, and quality applications Vault QMS, Vault QualityDocs, and Vault Training. Vault Quality and Vault RIM are part of Veeva MedTech, unified suites of cloud applications to manage regulated content and data throughout product development.
Watch the on-demand Veeva MedTech Summit session at veeva.com/MedTechSummit to learn how Epredia is streamlining quality and regulatory processes.
About Veeva Systems
Veeva Systems Inc. is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 950 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices throughout North America, Europe, Asia, and Latin America. For more information, visit veeva.com/eu.
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