Phase IIb/III Trials

Accelerate clinical trials with scale and precision

Success in Phase IIb and III clinical trials requires more than global reach, therapeutic expertise and operational excellence; it demands innovation. IQVIA’s advanced AI and technology help you navigate regulatory complexity, optimize enrollment strategies and drive patient engagement. With a global footprint spanning 100 + countries and access to diverse patient populations, we deliver measurable outcomes: faster timelines, reduced risk, improved quality and greater efficiency — so you can bring life-changing therapies to market.

Solutions Research & Development Clinical Trials Phase IIb/III Trials

Better protocol design starts here

Today’s clinical trials are more complex than ever. Phase III protocols alone now collect an average of 3.5 million data points. We can help you streamline your protocols for success with IQVIA’s unparalleled data — leveraging AI, automation and data captured at the point of care so you can design smarter trials.

End-to-end clinical development solutions

IQVIA delivers comprehensive solutions that optimize every step, from protocol design and study start-up to patient enrollment, ensuring speed, predictability, and operational excellence.

IQVIA offers:

Therapeutic depth and global/local expertise to navigate complex protocols.
AI-powered analytics for smarter site selection and patient recruitment.
Integrated study start-up services to reduce regulatory and contracting delays.
Tailored solutions for faster activation and more reliable outcomes.

The Result

Accelerated timelines, improved data quality, and precision-focused progress from pipeline to patient impact.

Project management as part of your team

Drive trial success with project managers who act as true partners from study planning through closeout.

Integrated project management

Our project managers work as extensions of your team — syncing with your workflows to develop trials on time, on target and in scope.

Smarter, AI-powered decisions

IQVIA project managers bring you proven sector expertise, industry-leading data science and IQVIA Healthcare-grade AI^® to power your trial.

Transparent, connected communication

We keep you in the loop with always-on communication, giving you insights into your trial’s progress every step of the way.

Data review that delivers confidence: Integrated and flexible solutions for cleaner data and faster database locks

High-quality data

Our expert-led, centralized data review ensures quality and consistency across the entire trial lifecycle — with built-in risk mitigation that accelerates timelines without sacrificing scientific rigor.

Bundled services

We eliminate the complexity of multi-vendor models by integrating Data Management, Biostatistics, Medical Safety Services, and Lifecycle Safety — an industry-leading connected approach.

Real-time visibility

Our workflow platform enables automated oversight, delivering real-time insights so you can make informed decisions.

End-to-end data flow

With all teams working from the same ecosystem, this level of integration provides a unified view of all data — offering a single source of truth for all functional roles.

Phase IIb/III trials solutions

Clinical Monitoring

Enhance patient safety and study quality by using data, analytics, and technology to monitor patient, site, and study performance with risk-based and centralized monitoring.

Lifecycle Safety

Harness the power of global human expertise combined with automation, artificial intelligence (AI) and machine learning (ML) to design, build and execute end-to-end safety solutions.

Regulatory Affairs

Navigate complex regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.

Medical Writing

Create transparency in your regulatory documents with a range of medical writing services that deliver quality and timeliness throughout your product development lifecycle.

Biostatistics

Getting the right outcomes from your clinical trials is all about the data and insights they provide. Biostatistics in clinical trials isn’t just a necessity, it can be a real competitive advantage.

Data Management

Ensure you have access to insights early with connected devices and clean, analysis-ready data