Efficient Regulatory Document Management
Veeva Vault Submissions is a robust content management platform that streamlines regulatory submissions by providing a comprehensive solution for planning, authoring, reviewing, and approving regulatory documents. With its enterprise capabilities, Vault Submissions simplifies the process of creation, version control, approval, and real-time co-authoring of all submission-related documents. This ensures that regulatory teams have a centralized platform to collaborate and manage their submission documents efficiently.
Advanced Features for Enhanced Productivity
One of the key features of Veeva Vault Submissions is its content planning capabilities, which allow users to create submission outlines and automatically match documents to the outline. Additionally, users can build and publish clinical and non-clinical reports using Report Level Content Plans, enhancing the accuracy and efficiency of document preparation. Dashboards and reports within the platform enable submission managers to monitor the status of each document in real time, providing insights into the progress of submissions and facilitating timely decision-making.
Benefits of Using Vault Submissions
By leveraging Veeva Vault Submissions, regulatory teams can benefit from a single authoritative source for all regulatory documents, ensuring consistency and accuracy in submissions. The platform offers actionable reports and dashboards that enhance visibility into submission progress, enabling teams to accelerate time to market by automating multiple authoring and assembly tasks. Moreover, Vault Submissions allows global teams to coordinate and align on submissions, streamlining interactions with health authorities and affiliate organizations. The platform has been proven to simplify and eliminate 80% of submission tasks, saving over 200 hours on approval and renewal reporting, while consolidating over 65 legacy systems.
Customer Testimonials and Industry Recognition
Leading organizations like Baxter have adopted Veeva Vault Submissions to drive global regulatory strategy and delivery. Customers have emphasized the importance of having a single source of regulatory truth, which Vault Submissions provides. The platform has been recognized for its ability to exceed expected outcomes by simplifying regulatory processes and saving significant time and resources. With a very mature status and over 100 customers worldwide, Vault Submissions is the go-to solution for efficient regulatory document management.
Resources and Further Learning
For those interested in exploring Veeva Vault Submissions further, resources such as product demos, white papers, and customer success stories are available on the Veeva MedTech website. These resources showcase how industry leaders like FDA, Bio-Rad, and Thermo Fisher are leveraging digital solutions to drive global harmonization and technological advancements in the medtech industry. Contact Veeva Systems to learn more about how Vault Submissions can revolutionize your regulatory processes and drive efficiency in your organization.