DATA MANAGEMENT
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.
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.
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.
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.
Advanced AI-Powered TMF Automation
Automate time-consuming manual processes with the industry’s only AI-assisted filing and indexing, increasing speed and quality.
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%.
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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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.
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.
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.
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.
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.
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.
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.
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.
The Transformation Of Clinical Data Capture And Management
Learn how the rapidly evolving clinical data capture landscape influences the challenges clinical data management teams face, and the emerging technology, processes, and skillsets that can help the industry adapt.
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.
Manage Exponential Data Growth With Medidata Clinical Data Studio
Bring study teams together like never before for total data quality oversight.
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.
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.
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).
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.
Trends In Clinical Transparency Policies
More and more sponsors are making their clinical trial transparency policy publicly available, says TrialScope Chief Strategy Officer Thomas Wicks. Hear additional disclosure and transparency trends.
The Future Of Clinical Data Management: Part 1: Too Fast, Too Furious
Medidata’s first webinar series for 2022 will bring industry leaders and game changers together to discuss the trends and insights in modernizing data management. This first webinar will provide best practices, practical tools and strategies that can be used today a...
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.
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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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.
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.