The Vault RIM Suite includes Vault Registrations, Vault Submissions, Vault Submissions Publishing, and Vault Submissions Archive for unified RIM capabilities on one cloud platform. More than 50 companies are using Veeva Vault Submissions Publishing to simplify and accelerate the submission process with assisted submission building and automated rendering of documents under existing standards. Vault RIM is also enabling companies with end-to-end submission development for faster time to market. The modernization effort helped to reduce SOPs and work instructions by over 90%, improving overall speed and agility. "Leveraging Veeva's advanced capabilities across our regulatory operations has helped to significantly simplify our processes, including nearly a 35% reduction in process handovers."Ī top 20 pharma used Vault RIM to harmonize more than 19 million data points and unify over 65 legacy systems onto a single cloud platform. Veeva Vault RIM has allowed us to consolidate data and documents from many different sources for greater visibility and efficiency," said Helen Donnelly, head of regulatory operations at Mundipharma. "Establishing one source for information was a top priority at Mundipharma. Non-eCTD electronic publishing to meet global submission requirements.Seamless connection with Veeva Vault PromoMats to send 2253-based submissions to Vault RIM.Active Dossier to manage chemistry, manufacturing, and controls (CMC) documents in effect for a given product and market.Veeva continues to deliver advancements that help customers streamline global regulatory processes. "More companies are relying on Veeva Vault RIM innovations to keep pace with regional and local regulations, and we're proud to support the industry as a trusted partner for advanced regulatory information management." "The rate of change across requirements and regulatory environments calls for agile systems that can adapt quickly," said Marc Gabriel, vice president, Veeva Vault RIM.
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