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.
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.
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.
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.
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.