Identify study quality and patient safety issues earlier.

Predictive analytics, artificial intelligence, and machine learning are enabling more precise decision making in clinical monitoring. See how centralized clinical monitoring from IQVIA can enhance study quality, add efficiency, and improve patient safety.
Contact Us

Mitigate risk, improve study quality

Clinical monitoring can account for up to 50% of study costs. IQVIA's clinical monitoring solutions integrate technology, data, analytics, and expert knowledge to create flexible, customized solutions that can reduce the cost of trial oversight by up to 25% - all while improving operations.  

female in an office working
female in an office working

More data, fewer issues

IQVIA's Risk-Based Monitoring (RBM) is proven to drive faster access to high quality data. With predictive and advanced analytics, you can identify and address issues earlier, creating efficiencies and improving safety for patients. Additional benefits include

  • In-depth, subject-level data to ensure medical congruency
  • Consolidated data on a single, automated platform
  • Demonstrated effectiveness for nearly all therapeutic areas and phases
IQVIA's Experience

300 studies

delivered using risk based monitoring across 39,000+ sites

Centralized meets risk-based

It takes both experience and technology to effectively maximize risk-based monitoring. Our centrally located clinical monitors continuously review and analyze data, including a subject-level review process, to deliver insights that identify and mitigate risks across sites and patients as well as the study itself.

Subject level data review early signal surveillance, KRI & trigger management, predictive & advanced analytics, targeted site support.

Automation drives excellence

IQVIA's centralized monitoring platform powers a more efficient approach to risk management by using automated workflows, resulting in 

  • Detailed transparency to trial status
  • Key risk indicator and trigger management
  • Enhanced data flow for increased compliance
patient listening to doctor
patient listening to doctor

Capabilities and outcomes

Combining risk-based and centralized monitoring enables subject-level surveillance and improves patient safety. Targeted site support enhances CRA efficiency. And the combination yields measurable improvements in outcomes.

Our Latest Thinking on Risk-Based Monitoring
Related solutions
Regulatory Affairs

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

Lifecycle Safety

Use AI, machine learning, NLP and new technologies to streamline pharmacovigilance, improve efficiencies, reduce costs, and meet safety demands.

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.

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.