DATA MANAGEMENT
Improving Supply Chain: Accountability, Sustainability, Optimization
Watch as industry experts explore the advancements in drug accountability facilitated through IRT, encompassing innovative methods for managing site variations and sustainable supply chains.
Overcome Data Challenges With Real-Time Workflows And Analytics
Explore how clinical teams can overcome data access and analysis challenges with real-time workflows, traceable decisions, and flexible analytics to accelerate insights and improve collaboration.
Castor eConsent: Site View
Study coordinators aim to enroll participants efficiently through a partnership that leverages direct-to-patient marketing to streamline recruitment.
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.
Yes, Your Study Is At Risk: Risk Mitigation Plans For Endpoints
Ocular endpoints often introduce unique bottlenecks that can stall enrollment and compromise data integrity. This presentation provides the tools for a streamlined, resilient clinical trial strategy.
Some Top Concerns When Implementing AI In Clinical Trials
Everything from fear of loss of personal privacy to risk bias can be a concern when implementing AI in clinical trials.
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.
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.
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.
Financial Scenario Planning — Budget With Confidence
Find out how financial scenario planning can revolutionize clinical trial budgeting with dynamic models, real-time data, and instant scenario visualization—all in one intuitive platform.
Trialtrove: Clinical Trial Data You Can Depend On
Trialtrove’s data, compiled from over 58,000 sources, helps study sponsors and CROs make informed decisions around clinical trial strategy, design, and execution.
How To Supercharge RWE Generation In Phase IV Trials
Watch as speakers discuss their joint efforts in implementing patient-centric digital trial solutions that harness the potential of RWD, translating it into actionable Real-World Evidence insights for a sponsoring client.
Why Veeva CDB
Watch a two-minute video to learn how Veeva Clinical Database (CDB) aggregates, cleans, and transforms clinical data from various sources, including third-party EDCs.
Helping Sponsors Keep Up With The Latest Clinical Trials Intelligence
Trialtrove helps sponsors form development strategy, anticipate competitive activity, benchmark trial designs and analyze trends. Sponsors also enjoy direct access to industry-leading analysts.
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.
Simple Description Of Clinical Analytics
Without teamwork, the best solutions still fall short. Unlock your clinical data's potential and transform chaos into clarity by starting with clear questions, adapting to insights, and fostering collaboration.
What Should You Ask The FDA About AI
Understanding what some of the common questions the FDA gets about AI may help you as you plan to interact with the agency.
Keeping Up With ClinOps: Why And How To Improve Delivery
Industry experts discuss the concept of a trial platform as a service and how it can accelerate and enhance the day-to-day functions of clinical operations throughout the entire lifecycle of a study.
Combining De-Identified EHR And Claims Data
Learn how EHR+ Data can improve your understanding of the patient's journey in ophthalmology, urology, and neurology clinical trials.
How FAIR Data Principles Power Clinical Analytics Success
Explore key challenges in accessing and preparing analytics-ready clinical data, how FAIR guiding principles can help maximize the value of clinical trial data, and the impact of innovative analytics.
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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What Is 'Fit For Use' In AI Models?
The data that you use to train AI models has to be “fit for use” according to the FDA. Tala Fakhouri explains what metrics the FDA uses to make this determination.
Medidata Clinical Data Management
By automating complex tasks, Medidata Rave simplifies clinical data management and capture. This leads to cleaner, more reliable data, allowing for quicker analysis and results.
psiXchange: Intelligent, Automated Safety Reporting
Say goodbye to manual burdens and embrace efficiency by fully automating your safety reporting. This will significantly cut down on effort and costs, all while enhancing compliance standards.
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.
Quality Insights For Ophthalmology Innovation
Verana Health provides data essential to answering your questions during the drug development process, particularly in the field of ophthalmology.
Accelerating Clinical Data Review With Traceable Workflows
Discover how streamlined workflows and enhanced collaboration between data managers and medical reviewers can boost clinical trial efficiency, improve data quality, and ensure patient safety.
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.
Collect Better Oncology Trial Data, Easier
In this webinar, experts discuss how enriching oncology clinical trials with RWD generates deeper insights and improves operational efficiency to achieve better patient outcomes.
Medidata Research Alliance
The Medidata Research Alliance collaborates with scientific and medical research communities to use clinical trial data for medical advancements and increased patient access to innovative treatments.