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RBQM 101: What Is Risk-based Quality Management?

Reading Time: 5 minutesThe adoption of RBQM in clinical trials has surged in recent years. According to a 2023 survey by the Tufts Center for the Study of Drug Development, sponsor and CRO companies are incorporating RBQM components in over half (57%) of their clinical trials. The most frequently cited challenges to RBQM implementation were a lack of […]

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Clinical Data Integration: Everything You Need to Know

Reading Time: 8 minutesSuccessful clinical trials rely on the collection and analysis of data from a wide variety of sources, including sites, patients, and labs, and linking clinical data to real-world data. Data collection typically comes from different systems and multiple vendors. Review and analysis are carried out by multiple stakeholders (data managers, CRAs, central monitors, medical monitors) […]

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The Benefits of AI in Healthcare: Reshaping Clinical Trials for Patients

Reading Time: 5 minutesArtificial intelligence is reshaping the design, planning, and execution of clinical trials. New efficiencies, capabilities. and opportunities are emerging everywhere: from early study design to data collection, trial operations, and beyond. As complexity increases and resources tighten, AI offers a new path forward—one that’s faster, more adaptive, and better-informed. Significant benefits for patients are expected […]

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Centralized Monitoring: A 360° Approach to Clinical Oversight

Reading Time: 7 minutesThe clinical trial industry is facing several challenges today. Increased protocol complexity makes it harder to enlist sites that can deliver patients and high-quality data. Patient retention remains an obstacle despite the flexibility provided by remote and decentralized data collection. The variability of data sources and an increased number of stakeholders are creating a significant […]

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Oncology Imaging in Clinical Trials: The Latest Tech Innovations

Reading Time: 2 minutesImaging plays a pivotal role in oncology clinical trials. It’s essential for evaluating tumor burden, assessing treatment response, and tracking disease progression. But traditionally, imaging workflows have been manual, variable, and time-consuming challenges that can delay trials and complicate regulatory submissions. Today, that’s changing. Technology is transforming the imaging landscape—delivering faster, more consistent, and higher-quality […]

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The Advantages of AI for Clinical Trial Sites

Reading Time: 5 minutesSites are the core of every clinical trial. But in today’s environment with limited resources and increasingly complex protocols, they need stronger partnerships and better support. This doesn’t mean inundating site staff with as many technologies and tools as possible, however. Instead, they must be strategically empowered to spend more time on the tasks that […]

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Medidata to Join Forces with Dassault Systèmes, Creating the First End-to-End Scientific and Business Platform for Life Sciences

Reading Time: < 1 minuteAccelerating the digital transformation for Life Sciences has been our sole focus and commitment during the past 20 years. For pharmaceutical, biotech, and medical device companies, the promise of delivering precision medicine – with data-driven, insights-led decisions in real-time, and a full lifecycle platform to manage all data and operations – is paramount. That’s why […]

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Patient Payment Optimization: The Challenges &#038; Opportunities

Reading Time: 5 minutesFlexibility, transparency, empathy, and a sense of shared purpose were key components for success when it comes to patient payments—based on a recent conversation between experts who live it every day: patients, sites, and sponsors. Earlier this year, Medidata hosted two in-person Patient Payments Workshops where pharma and biotech leaders got to talk one-on-one with […]

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Clinical Data Management: Everything You Need to Know

Reading Time: 11 minutesClean, consistent, high-quality data is the lifeblood of a clinical trial. Clinical data management (CDM) is the collection, validation, quality management, integration, and delivery of clinical data to deliver high-quality, reliable data for statistical analysis, regulatory compliance and submission, medical decision-making, and further clinical research. Originally, CDM was manual, paper-based, and error-prone. In the 1990s, […]

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Marisa Co Talks AI, DCTs and the Future of Life Sciences

Reading Time: 5 minutesWelcome to the Clinical Minds “Innovator Insights Corner,” where we’ll be sharing fascinating stories, perspectives, and predictions from the guests of ‘from Dreamers to Disruptors’, a podcast by Medidata exploring life sciences innovation and the visionaries behind it all. Healthcare and technology have always been closely related. New developments in data management and analysis have […]

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