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Reading Time: 2 minutesWhen recruiting patients and running a clinical trial, it’s ideal to enroll patients that represent the broader population to the closest extent possible. But this is not always feasible. Recruiting any patient to a clinical trial is challenging—achieving diversity and assembling a patient pool that accurately reflects real-world demographics poses additional hurdles. Underrepresented demographics in […]

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Reading Time: 6 minutesMedidata would like to thank attendees who participated in the 3rd annual Optimizing Your Endpoint Adjudication Process Today and Beyond virtual experience. This event brought together industry leaders and colleagues to discuss key aspects of endpoint adjudication in clinical trials. This year, two expert panels shared their knowledge of common pitfalls and best practices in […]

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Reading Time: 2 minutesThis blog was authored by Matt Noble, SVP, Product Management, Patient Cloud at Medidata. DCTs! Sensors! ePROs! All represent crucial elements to cultivating more patient-centric experiences in clinical trials. To get there, we rely on the extensive knowledge and expertise of investigators, clinical operations and regulatory professionals, patients, advocates, and everyone else in-between. There’s one […]

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Reading Time: 5 minutesIn June 2024, Michael Peel, Science Editor of the Financial Times, moderated a FT LIVE webinar in partnership with Medidata, Transforming the Clinical Research Experience. This must-watch session featured key speakers representing patients, research sites, sponsors, and Medidata. The panel’s unified message is that the transformation of the clinical trial experience begins with listening and […]

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Reading Time: 4 minutesThis blog was authored by Freddy Mendieta, Director, Product Management, Coder/Coder+/Safety Gateway at Medidata. Life sciences companies are seeking ways to harness new technologies like AI/ML. There’s a mix of emotions ranging from excitement to hesitation about using these technologies. Let’s explore some of the challenges and benefits—while keeping in mind the goal of helping […]

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Reading Time: 5 minutesImagine a clinical research ecosystem where data flows seamlessly, experiences are unified, complexities are minimized, and teams can focus on what truly matters: driving scientific breakthroughs. Enter Medidata Clinical Data Studio. More than a tool, it’s a transformative approach to redefining how data is managed across an ever-growing volume of sources. Sharlene Carnegie, SVP, Engineering […]

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Reading Time: 9 minutesDiscover the essentials of electronic clinical outcome assessments (eCOA) and learn how eCOA enhances patient experience, data accuracy, and operational efficiency.

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Reading Time: 2 minutesPatients who participate in clinical trials are rarely connected to their routinely collected real-world data (RWD). Patients generate health data throughout their lives, whether it be from labs, hospital visits, pharmacy prescriptions, or health records. Data collected during clinical trials, however, typically offers just a snapshot of a patient’s health at specific points in time—without […]

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Reading Time: 5 minutesHearing a leader from the clinical trial research site community describe the site experience as trying to “break out of the escape room” is enough to give anyone pause for thought. The commenter was Viviënne van de Walle, co-founder of the independent clinical research site, PT&R, and a member of the leadership council for the […]

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Reading Time: 5 minutesArtificial intelligence (AI) has become quite the buzzword over the past couple of years, and for good reason. We’ve seen significant advances both in how compelling AI can be – from writing a bedtime story to composing a tweet – and the impact it can deliver in almost every sector, from driving cars to providing […]

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Reading Time: 2 minutesThe benefits of implementing AI into the clinical trial process are promising—potentially mitigating prevalent concerns surrounding data privacy and protection. In traditional clinical trial settings, companies are understandably hesitant about sharing clinical trial data due to the fear of violating patient data privacy or any of the strict data protection laws. It’s widely known and […]

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Reading Time: 4 minutesThe clinical trial landscape has become increasingly complex, resulting in fewer study starts, longer approval timelines, and greater budget cuts—ultimately challenging organizations to do more with less. Discover why sponsors are adopting data linkage to tackle the challenges of longer timelines, complex trials, and high costs in clinical development—and learn how linking clinical trial data […]

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