IQVIA empowers the life sciences industry with cutting-edge analytics, innovative technology solutions, and comprehensive clinical research services on a global scale. IQVIA ePromo is a highly scalable, cloud-based content management system (CMS) solution that addresses your organization’s growing commercial content demands. Rise above the challenges of the rapidly evolving digital landscape and content globalization with ePromo’s sophisticated features and out-of-the box configurations based on industry expertise, adapted to your needs.
ePromo Cloud-Based CMS for IQVIA
About the Project
The request was to develop a content management system tailored to the unique demands of reviewing and approving pharmaceutical advertisements. The goal was to create ePromo, a cloud-based CMS designed to streamline complex workflows for managing advertising claims. This system enables users to annotate advertisements and seamlessly link claims to supporting reference materials. Built with deep industry expertise, ePromo is adaptable to IQVIA’s evolving content management needs in a dynamic, globalized market.
The challenge lied in managing the complex process of reviewing and approving pharmaceutical advertisements. A content management system had to handle stringent regulatory requirements, streamline workflows, and ensure seamless collaboration across teams. As IQVIA’s clients operate worldwide, the solution is supposed to be highly scalable and adaptable due to advertising standards. Moreover, various regional regulatory requirements need to be taken into account. Structured claims tracking and evidence linking were challenging for the solution.
Danavero built a system that is used for clients to review and approve pharmaceutical advertisements. This area of the industry is mostly self-governed in an adversarial fashion (i.e. pharmas check each other's advertisements). Each advertisement can make some number of "claims" about a drug/product, but which must be backed up by some reference material. The ePromo system allows for medical, legal, and regulatory reviewers in a pharma to mark up advertisements with comments, and for the workers managing the process to track the claims made in an advertisement, and how they link to evidence.