Regulatory Affairs

Focus on research, not regulations.

Address increasingly complex regulatory issues and stay ahead of changing requirements using integrated data and systems, global presence and expert advice. IQVIA can help you build a regulatory strategy, develop global clinical and regulatory plans and execute on your marketed product maintenance requirements so you can focus on research and development.

Regulatory Affairs

Driving regulatory strategy through insights

IQVIA's Regulatory Affairs and Drug Development Solutions integrates technology, analytics, and insights built from years of experience to help biopharma companies exceed global compliance goals, reduce costs and get drugs to market faster.

Our offerings span the drug development continuum where our assistance with the creation of a regulatory strategy and development plan helps eliminate surprises, keep development on track, and ensure appropriate quality strategy at each step.

Tech-Enabled Regulatory Affairs

Enhance regulatory productivity through automation

Intelligent regulatory systems, robotic process automation and mobile access are changing what’s possible. IQVIA gives you turnkey access to business-transforming technology, including

  • Document comparison tools that make diagnostic efforts easier
  • Structured content authoring capabilities to help manage data in submissions
  • Automation of duplicative, high-effort, low-complexity tasks

At IQVIA, we are also combining multiple capabilities into customized expert systems to enhance productivity to help reduce the burden of administrative tasks.

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