Solving Pharma’s Content Efficiency Problem with Veeva & GlobalVision

Overview

Proofreading critical content accurately and at scale is a major concern in the Enterprise Pharma and life sciences industry though, currently, content and documentation checks are still mainly done manually. This is otherwise extremely tedious, time-consuming, and with a high margin for human error.

Veeva, the leader in cloud-based software solutions for the life sciences industry and Veeva’s Silver Status Technology partner, GlobalVision, together have found an answer to this problem— an end-to-end solution for regulated industries to scale the creation, review and distribution of highly critical content.

Register for our webinar to learn:

• How Veeva and GlobalVision are empowering users to perform fast and accurate inspections that detect all text and artwork errors without having to download documents
• How this technology alliance addresses the gaps in MLR, DAM and RIM to reduce the chance of errors being created with every change or handoff
• How one of the world’s largest enterprise pharmaceutical brand leverages the Veeva and GlobalVision integration for cleaner handoffs and to reduce the overall number of revisions, minimize cycle time, and get products to market faster without compromising quality

Save your seat for our upcoming webinar!