DATA MANAGEMENT
The Many Facets Of Early Phase Evaluation Of Psychedelics In Psychiatry
Altasciences and Sygnature Discovery discuss the clinical and non-clinical studies required for evaluation of abuse risks of psychedelic drugs.
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.
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.
Unlock The True Power Of Clinical Research Data With Clinical Data Studio
Discover Medidata Clinical Data Studio—where seamless data integration meets AI-powered efficiency. Accelerate reviews, manage risks, and enhance patient safety with a unified view of all your clinical data.
TRACON: Reducing Clinical Trial Cost By Connecting Systems
Companies are gaining operational efficiencies with a single platform across R&D including CTMS, EDC, and Safety. Hear how one biotech is breaking down system silos and eliminating data reconciliation, reducing clinical trial costs by 70%.
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.
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.
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.
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.
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.
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 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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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.
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.
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.
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.
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.
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.
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.
Advanced AI-Powered TMF Automation
Automate time-consuming manual processes with the industry’s only AI-assisted filing and indexing, increasing speed and quality.
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.
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.
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.
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-...
Day In The Life Of A Data Manager
Explore this patient data surveillance (PDS) solution — which is part of Medidata Detect — and how it's providing a single workspace for CDMs to aggregate, anatomize, and review patient data from multiple sources.
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).
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.
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.
Using Data To Accelerate Racial Diversity In US Clinical Trials
Historically, US clinical trials have been shown to recruit disproportionately large percentages of White patients, raising concerns about the generalizability of clinical trial results to underrepresented racial minority patient populations. Because of this, the FDA has ...
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.