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.
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
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.
IQVIA's centralized monitoring platform powers a more efficient approach to risk management by using automated workflows, resulting in
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.
Lessons learned from navigating through a global pandemic.
The global pandemic: a catalyst for long overdue changes in clinical trial monitoring?
COVID-19 is driving change in clinical development, bringing trials closer to patients and expanding regulatory guidance to include virtual trial capabilities – from remote monitoring to telemedicine, direct-to-patient shipment of investigational medicines and the use of home health nurses in clinical research.
Navigate complex regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.
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.
Create transparency in your regulatory documents with a range of medical writing services that deliver quality and timeliness throughout your product development lifecycle.
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