DATA MANAGEMENT
Better Data Strategies: Best Practices For Integrating And Analyzing
In this panel discussion, we explored best practices for integrating and analyzing data to support informed decisions, including how ICH E6 R3 defines risk-proportionate approaches in clinical trials, what that means in practice, and how sponsors and sites can adapt. You ...
Leveraging AI And Machine Learning To Deliver Next Generation Feasibility & Site Selection
In this presentation delivered at SCOPE 2022, hear how ICON leveraged Study Feasibility to its advantage.
Patient-Level Clinical Trial Data + Real World Data
Future-proof your clinical trial and enhance your evidence generation activities with Medidata Link, which allows sponsors to collect clinical trial data and link it at the patient level to real-world data (RWD).
Trends In Clinical Transparency Policies
More and more sponsors are making their clinical trial transparency policy publicly available, says TrialScope Chief Strategy Officer Thomas Wicks. Hear additional disclosure and transparency trends.
5 Strategies To Dramatically Improve Clinical Data Quality
Discover how to unify data management and risk-based quality management approaches and augment processes with automation and AI to find and fix data quality issues sooner and more efficiently.
Clinical Trial Disclosure, Transparency & Data Sharing – A Lifeline For Medicine
When Craig Lipset talks pharma, people listen. The former Head of Clinical Innovation and Venture Partner at Pfizer shares his insights on clinical trial transparency and is joined by Chris Boone of AbbVie in a fireside chat.
Qdata From Verana Health For HEOR And Medical Affairs
Obtain real-world data on patient demographics, treatment patterns, and outcomes to help inform your future business decisions.
Clinical Analytics Use Cases For AI
Automating FDA data validation rules and analyzing audit trail data can significantly reduce fraud and predict areas of concern. Discover how these advancements can transform your clinical trials.
Streamline The Clinical Trial Disclosure Process
Core Data simplifies the registry submission and approval process by consolidating data for multiple registries into one single form, promoting consistency across registries and saving time by minimizing data entry.
Improving Safety Reporting Speed And Accuracy With Automation And Embedded Intelligence
Watch this exploration of real-world case studies of companies utilizing intelligent process automation and embedded, regularly updated safety reporting regulatory intelligence of psiXchange software.
Providing Rich Quality Data In The Neurology Space
From clinical development to post-approval, we provide quality insights powered by the Axon Registry through our exclusive partnership with the American Academy of Neurology.
Sitetrove: Industry-Leading Global Investigator And Site Intelligence
With over 500,000 investigators and more than 180,000 clinical trial sites spanning 185 countries, Sitetrove provides the data vital to accurately assessing target locations, identifying qualified investigators, and prioritizing candidates for clinical trial success.
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2 Of The Most Impressive AI Applications
Elena Sinclair reveals the only two (out of 12) applications of AI in clinical development that McKinsey identified as decreasing costs, improving timelines, and increasing probability of success.
Addressing Opportunities And Challenges In Digital Health Data
Experts from diverse industry sectors unpack key points from the FDA’s final guidance on Digital Health Technologies (DHT) for remote data collection in clinical investigations.
Manage Exponential Data Growth With Medidata Clinical Data Studio
Bring study teams together like never before for total data quality oversight.
Reporting To ClinicalTrials.gov: Reflections And Challenges
Who can reflect better on this topic than Dr. Deborah Zarin, former director of ClinicalTrials.gov? Dr. Zarin, now with the MRCT Center, shared her experiences and advice at the recent EXTRA: TrialScope Transparency Experience.
Improving The Quality Of Submitted Studies To ClinicalTrials.gov
Want to reduce QC comments? Hear tips from Dr. Deborah Zarin, former director of ClinicalTrials.gov, now with the MRCT Center. Dr. Zarin was keynote speaker at the recent EXTRA: TrialScope Transparency Experience.
Global Compliance Made Easy
Global clinical trial disclosure compliance is inherently complex, with over 39 registries, Most sponsors simply lack visibility into all the places they need to disclose information or what their commitments are. Automation can help make global compliance easier.
The New Era Of Evidence Generation In Clinical Trials
Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.
Amplifying Evidence With Unified Clinical Trial Data Collection
In this presentation, we explore the transformative potential of integrating a unified clinical trial data collection platform with intelligent automation, challenging the inadequacies of the status quo.
Harnessing The Potential Of Patient-Level Data In Clinical Trials
Join our panel of industry leaders as they explore innovative methods and best practices for incorporating fully consented patient data in clinical trials.
The Importance Of Reliable Data To Clinical Trial Activation
Find an easier way to identify and enroll eligible patients for your clinical trials with quality data and site selection.
A Framework For Selecting Reliable Clinical Endpoints From Real-World DHT Data
Dr. Andy Liu presents a case study determining which digital measure of physical activity would be a well-defined and reliable clinical endpoint in a trial including patients with diabetes.
The Role Of Technology In Improving Site Performance
Explore how clinical trial sponsors can benefit from the growing use of electronic source (eSource) technology at research sites.
Accelerating Data Cleaning
AI-enabled clinical trial technology enables faster processing of large data volumes, thereby enhancing workflows, easing the burden on busy trial teams, and protecting patients.
AI In Clinical Trials What's New And What's Hype
Our third Clinical Leader Live on AI will go beyond the buzzwords to focus on what’s actually working in clinical operations.
Accelerate Clinical Insights: From Data Deluge To Decisions In Minutes
Unlock clinical trial insights in minutes, not months. Discover a platform that streamlines data review with AI-powered listings and visualizations to empower faster, smarter decisions.
Clinical Data Studio: A Single Data Review Platform Fostering Unification Across Groups
This end-to-end digital review platform can assist both your risk management team and data management team, improving speed and facilitating database lock times.
A Framework For Scalable Clinical Trial To Real World Data Linkage
Discover a scalable framework for data linkage in this on-demand webinar. Learn strategies to efficiently manage large datasets, enhance accuracy, and overcome common challenges in data integration.
Evolving Data Review With AI
AI is transforming clinical data review by automating processes and enhancing efficiency. Discover the four stages of evolution that emphasize automation, regulatory alignment, data analysis, and human oversight.