Europe, Middle East & Africa
Simpler at every step.
Streamline your regulatory compliance systems and processes with our new end-to-end regulatory technologies, advisory and tech-enabled services. Free your team from labor-intensive tasks and maintenance to focus more on delivering valuable products to market.
>2K regulations
NEW OR MODIFIED, RELEASED BY THE FDA ALONE SINCE 199853% of CEOs
In global life sciences consider industry regulations a top disruptive business trendExplore our comprehensive regulatory capabilities
Regulatory compliance has long been viewed as a cost center and a necessity, but leading organizations are recognizing opportunities for innovation in this space.
Ronan Brown, SVP & Head, IQVIA Integrated Global Compliance
Affordably improve publishing and e-submission cycle times with IQVIA Regulatory Productivity Tools.
IQVIA’s new Regulatory Productivity Tools make authoring and PDF publishing fast and efficient. And our validation tool ensures that what you submit to regulatory authorities is in technical compliance prior to dispatch.
- More easily prepare, publish, and validate eCTD and Non-eCTD electronic submissions
- Increase efficiency and reduce associated infrastructure costs
- Maximize throughput with intuitive, well-designed interfaces
With comprehensive RIM systems, companies gain much greater insight into their regulatory programs.
RIM Smart – an intelligent, integrated approach to regulatory management.
RIM Smart is the modern regulatory information management solution built to increase speed, collaboration, efficiency and visibility across your entire global portfolio, improving performance at a lower cost.
Delivered securely in the cloud, IQVIA RIM Smart provides interconnected, comprehensive and intelligent management of the entire regulatory process.
A single source for information and implementation
IQVIA RIM Smart
In future, authors’ and publishers’ jobs will be transformed by artificial intelligence with algorithms custom-built to manage the routine work, freeing up professionals to focus on higher-value activities.
DEVJANI GHOSH DASGUPTA, PhD Director
Global Regulatory Affairs
Lower administrative burden across the product lifecycle with IQVIA’s Global Regulatory Affairs services
Our experienced GRA team helps biopharma and medtech companies handle regulatory workflows more flexibly, productively and efficiently. From strategic regulatory advice to regulatory maintenance and lifecycle support, we’ve got you covered. IQVIA’s expert resources, streamlined processes and leading technologies provide
- Optimized time to key decision points
- Regulatory and operational risk mitigation
- Streamlined regulatory pathways
- Flexible approaches to generating more informative evidence earlier
- Improved transparency and proactive problem-solving
Engage local resources to cope with variable demand
Dealing with workload peaks can be difficult—and expensive. Deploy trusted IQVIA resources to meet your needs around the world and allow your in-house professionals to focus on innovation and strategy. Scale quickly and reduce fixed costs by using our local, highly skilled, knowledgeable professionals to handle your work—on-demand.
Boost your compliance performance through RIM
How an agile approach can drive change management, increase user buy-in, reduce risk and ensure added value
How AI will significantly cut turnaround in the regulatory publishing workflow
