DATA MANAGEMENT
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.
Disclosure & Transparency Trends Webinar
Hear results from TrialScope’s 2019 Global Clinical Trial Disclosure & Transparency Benchmark Survey, highlights from our Plain Language Summaries Survey, and predictions for 2020.
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.
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.
Revolutionize Data Access With An AI Powered Custom Listing Generator
Clinical teams can now access trial insights in real time using natural language to streamline workflows and accelerate decisions. Discover how to bridge data gaps with AI-powered tools.
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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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.
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.
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.
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.
Verana Health: Where Quality Powers Insights
Drive innovation by improving your digital health in ophthalmology, urology, and neurology.
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.
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.
The FDA's View Of AI In Clinical Trials Is Limited
Tala Fakhouri explains that there could be so many more applications of AI in clinical development than what the FDA sees in regulatory submissions.
Leveraging DHTs To Improve Data Collection And Analysis
How can wearable DHTs be leveraged to measure physical activity in patients with immunological diseases, enhancing clinical trials and advancing drug development?
AI In Action: Transforming Clinical Trials
Tala Fakhouri, associate director for data science and ai policy at the FDA, along with industry consultant Elena “Ella” Sinclair of FlexPoint Bio, talk about common applications of AI in clinical development and the new AI-focused regulatory Guidance from the...
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.
TMF Migrations: Streamlining The Journey To An Inspection-Ready Result
Delve into several techniques designed to safeguard data precision and integrity throughout the TMF migration process, reducing compliance risks and conserving valuable time and effort.
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.
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.
How ICH Oversight And AI Are Shaping The Future Of Clinical Trials
Explore how the new ICH E6 (R3) revisions are reshaping clinical trial oversight and examine how AI-driven tools like the Clinical Decision Suite can help sponsors enhance trial efficiency.
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.
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.
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.
Importance And Requirements Of Study Results Posting
In addition to laws requiring disclosure of clinical trial results, the public also demands this information. TrialScope Chief Strategy Officer Thomas Wicks explains why sponsors should share study results.
Modernizing Clinical Research With AI And Digital Data
Discover how ActiGraph is revolutionizing clinical trials with patient-focused digital data and cutting-edge technology that enhances trial efficiency across all phases.
Utilizing Curated Data To Boost Your Urology Research And Innovation
Obtain robust data from a reputable source to boost your urology research and propel your life science company's innovation in the urology space.
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.
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).
Pharmaprojects By Citeline
With Pharmaprojects, leverage your mastery of the R&D space to create winning strategies, identify the right drugs to license, and support the key decisions that will drive your company forward.