DATA MANAGEMENT
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.
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.
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.
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.
Castor eConsent: Site View
Study coordinators aim to enroll participants efficiently through a partnership that leverages direct-to-patient marketing to streamline recruitment.
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.
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.
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 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.
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?
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.
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-...
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.
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.
Here To Help You Succeed
IQVIA Biotech is a standalone business of IQVIA with dedicated teams delivering clinical development solutions for biotech and emerging biopharma customers. Discover why IQVIA Biotech is the CRO partner of choice for biotech companies around the world.
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.
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.
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.
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.
Case Study: Optimizing Clinical Supply Chain With Advanced Technology
In this interactive discussion, IQVIA Technologies' IRT experts delve into real-world examples and practical AI applications.
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.
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.
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.
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.
Verana Health: Where Quality Powers Insights
Drive innovation by improving your digital health in ophthalmology, urology, and neurology.
How To Boost Disclosure Efficiencies With Outsourcing
In this webinar, you’ll hear about exciting new advisory and managed disclosure services from TrialScope, including: compliance, policy and process assessments, as well as plain-language summaries, protocol registration, results posting, and redaction services.
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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.
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.
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.
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.