DATA MANAGEMENT
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.
How Data Impacts GBM/RGB Clinical Trials?
In this video, Elizabeth Lamont, Senior Medical Director for Medidata AI, describes how an external control arm can be used in rGBM/GBM and the advantages of using an AI SCA, built upon historical clinical trial data.
How Biotech Gets Built With Professor Justin Stebbing
Navigate the complexities of biotech innovation by exploring how AI, the GLP-1 revolution, and shifting global trial trends are redefining the path to safer, more effective patient treatments.
Beyond The Data Deluge: Immune Profiling In Early Immuno-Oncology Trials
This presentation explores how to design effective immune monitoring for early-phase immuno-oncology trials, focusing on strategic platform selection, cost, and operational feasibility.
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.
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 Evolving Role Of AI And Innovation In Cardiac Monitoring
In this presentation, the panel of experts focuses on the changes AI has brought to cardiac monitoring data during clinical trials and addresses the skepticism over the use of new innovations.
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.
Streamline EDC Data Entry Using EHR Data
Explore how a clinical research coordinator (CRC) typically manually re-enters data from their EHR/EMR system into Rave EDC, and how Rave Companion provides automated assistance to enable the CRC to complete EDC forms.
The Impact Of AI On Mobile Visits
Experts discuss the FDA's new AI guidance, global harmonization, and the ethical implications of AI in clinical trials. Discover the challenges and opportunities ahead.
Make Sense Of Unstructured Data In Neurology, Urology, and Ophthalmology
Transform your data and, ultimately, patient outcomes across three major therapeutic areas: Neurology, Urology, and Ophthalmology.
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.
Citeline Study Feasibility
This predictive analytic solution helps sponsors select global study sites to successfully enroll more patients and accelerate clinical trial cycle times. Study Feasibility leverages both human expertise and machine-learning algorithms trained on Citeline’s best-in-...
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.
Keys To Successful Clinical Trial Data Handling And Re-use
In this video, Matt DeFranco, TrialScope Director of Solution Engineering, explains ETL (extract, transform, load) and API (application program interface). He then provides two case studies on their use in clinical trial disclosure and patient engagement.
Manage Exponential Data Growth With Medidata Clinical Data Studio
Bring study teams together like never before for total data quality oversight.
Beyond Clinical Trial Disclosure – The Ethical And Business Demands For Clinical Trial Transparency
The COVID-19 pandemic brings to light the ethics of getting information out more quickly than strictly required by regulation, or more thoroughly, as medical professionals, media and the general public are all looking for effective and safe treatments.
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 Cutting Edge Of Pharma: AI And RWD
Taken from a spotlight session at the CNS Summit, gain insights from thought leaders from Norstella and Citeline regarding artificial intelligence and real-world data.
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.
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.
Verana Health: Where Quality Powers Insights
Drive innovation by improving your digital health in ophthalmology, urology, and neurology.
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.
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.
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.
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.
Advanced AI-Powered TMF Automation
Automate time-consuming manual processes with the industry’s only AI-assisted filing and indexing, increasing speed and quality.
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.
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.
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.