Efficient, accessible, and orchestrated content - at the right time. 

Move to streamlined processes for clinical, commercial and regulatory content. End-to-end solutions from IQVIA are orchestrated to integrate intelligently with your environment, automating processes and simplifying content management with built-in compliance.
Contact Us

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 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

IQVIA helps you take control of content management issues

Greater need for collaboration, disconnected legacy platforms, actionable data and insights, exponential content growth, heightened compliance risks
Greater need for collaboration, disconnected legacy platforms, actionable data and insights, exponential content growth, heightened compliance risks
commercial content management suite
commercial content management suite


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.

leading meeting
leading meeting

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.

Learn more

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.

Safety, Regulatory, Quality and Commercial 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.

Contact Us
Contact Us
Contact Us

Email Us

Get in touch today to discover the right solutions for you.

Call Us

We are pleased to speak with you during our standard business hours.

U.S. Toll-Free only
+1 866 267 4479

For international call please find a number in our toll-free list.