Europe, Middle East & Africa
Efficient, accessible, and orchestrated content - at the right time.
More control for information intensive enterprises
Modern pharmaceutical and medical device companies create and manage immense amounts of business-critical content across the product lifecycle. There’s no compromising on compliance, but there is a way to manage risk and decrease the effort required to create, approve, and disseminate regulated content.
IQVIA's secure, cloud-based content management solution empowers you to replace multiple systems and workstreams with a single end-to-end platform, establishing a common source for business-critical clinical, commercial compliance and regulatory content. IQVIA content management delivers enterprise-wide content at the most granular level, at the right time. So everyone, everywhere has access to the same information on the same platform at the same time.
- For research , IQVIA eTMF lets you be inspection-ready, and helps anticipate issues before they become problems
- For commercialization, IQVIA ePromo gives you visibility and accountability across your markets
- For regulatory content submissions, IQVIA eREG supports streamlined content creation, organization and approval for submission documents in accordance with the requirements of health authorities around the world
Manish Goel, VP & General Manager, Content ManagementIntuitive content management with orchestrated workflows and built-in compliance, improves efficiencies and processes across the product lifecycle.
IQVIA helps you take control of content management issues
Solutions
Manage research efficiently and accurately across multiple trial sites. IQVIA's integrated content management suite eliminates barriers to collaboration and improving inspection readiness and accountability, which can help eliminate inefficiencies and improve transparency.
Control approvals with commercial content management
Track and manage review, approval, certification and dissemination of materials to support compliance, with one system. IQVIA enables global collaboration, review and standardized reporting, which can shorten approval cycles and make compliance cost-effective.
Control submissions in regulatory information management
Manage regulatory information, from correspondence and commitments to submissions, registration and tracking. IQVIA lets you eliminate most manual data entry and do away with spreadsheets, which makes the process not only more efficient, but more scalable across sites and countries.
Implementation to fit your organization
IQVIA provides global technology rollout and maintenance support to seamlessly integrate content management solutions with your existing technology architecture. IQVIA offers extensive consulting and service capabilities to meet the most complex organizational requirements.
IQVIA’s healthcare experience informs platform customization based on your business structure, products and locations.
Manage trial master files from planning through archive with solutions designed to improve workflow efficiency, promote collaboration, and support compliance.
Explore how ePromo can help manage promotional and medical information assets across the full content lifecycle, from creation to expiry to withdrawal.
Get an overview of IQVIA's full range of solutions to help you work more efficiently, standardize and improve controls across development stages and geographies.