Empowering Transformation Through Technology
From Clinical Data Management to Clinical Data Science
Amidst constant dynamic changes in clinical trials, the paradigm of traditional clinical data management, from technology to processes, is quickly shifting to an insight-driven, risk-based clinical data science approach.
Clinical data management has traditionally been responsible for clinical trial integrity, from collection to delivery for statistical analysis in support of regulatory activities. It ensures the accessibility, accuracy, and security of data, focusing on its organization, maintenance, integrity, and compliance with regulatory standards
Evolution of AI in Healthcare and Clinical Research
If asked about the origins of artificial intelligence (AI), what comes to mind? For many, sentient robots or non-human entities from science fiction books and films are the embodiment of AI. Think of Maria in Metropolis (1927), HAL 9000 in 2001: A Space Odyssey (1968), C3PO in Star Wars (1977), and Terminator (1984), to name but a few. For others, especially given the amount of news coverage about large language models (LLMs) at the moment, ChatGPT will immediately spring to mind.
Recently Published: Study of Novel Surface Electromyography Sensor
Nature recently published a study in which Medidata worked to establish the validity and reliability of the BioStamp nPoint biosensor for measuring electromyography in individuals with cervical spinal cord injury (SCI) by comparing the surface electromyography (sEMG) metrics with the Trigno wireless electromyography system
Medidata Launches Clinical Data Studio, Leveraging AI to Modernize the Data Experience in Clinical Trials
New York – June 18, 2024 – Medidata, a Dassault Systèmes brand and leading provider of clinical trial solutions to the life sciences industry, today announced the launch of Medidata Clinical Data Studio, a unified experience that unlocks the true power of clinical research data. This groundbreaking technology gives stakeholders greater control over the quality of data and the ability to deliver safer trials to patients faster.
NEXT New York 2024
Medidata NEXT returns to the Sheraton New York Times Square on November 13–14. And we’re bringing the unmistakable energy and innovation that makes NEXT so special. The biggest life sciences names, the most pressing topics—all tied together by immersive clinical trial experiences.
Come together with your peers to share solutions to life sciences’ biggest challenges, learn from top organizations, and explore how technology is improving clinical research across all stakeholders—from patients, to sites, to sponsors, and CROs.
Knowledge Hub: What’s New
When you search Medidata’s product documentation on the Knowledge Hub, do you always use the same filters to narrow your search results? Check out the latest Knowledge Hub blog post on setting your search preferences and find the content you need even faster!
Clinical Minds Blog
Be sure to bookmark the Clinical Minds Blog webpage and check back frequently for our latest industry insights.
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Meet Our Subject Matter Experts
Paul O’Donohoe
Senior Director, eCOA Product and Science
Paul O’Donohoe is Senior Director, eCOA Product and Science at Medidata Solutions, a clinical software platform provider. He is responsible for providing strategic oversight of the development of Medidata's electronic clinical outcome assessment technologies, and supporting internal teams and partners around the implementation of industry, regulatory and scientific best practices in clinical trials using mobile health technologies. He is passionate about developing the field of eCOA and mobile health through research and active involvement in industry consortia, and was previously the Industry Vice-Director of the C-Path ePRO Consortium.
Previously, Paul worked as a research psychologist at a child and adolescent mental health clinic based in Dublin, Ireland. He moved into the health consulting field with United BioSource Corporation where he worked across the health outcomes, health economics and health data capture groups. Prior to Medidata, Paul was Director of Health Outcomes at CRF Health (now Signant Health), an eCOA provider, where he led their health outcomes team. He has a MSc in Cognitive and Clinical Neuroscience.
The Latest from Dassault Systemes
Navigating the Complexities of Documents in CMC Dossiers: The Power of Structured Documentation
A study published in the Journal of Pharmaceutical Sciences offers a compelling outlook on the future of CMC regulatory submissions. Researchers predict a shift from traditional documentation to structured content and data management (SCDM) for dossiers. This strategic transition is anticipated to significantly streamline the process of CMC regulatory submissions.