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
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.
With comprehensive RIM systems, companies gain much greater insight into their regulatory programs.
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.
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
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
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.
Quality, regulatory, safety and compliance solutions across the device lifecycle.
Harness the power of automation to execute streamlined end-to-end safety solutions while reducing costs.