E-TECHNOLOGIES
Unleash The Power Of IQVIA eCOA: A Deep Dive
Edward Bartels, an expert in eCOA solutions, provides an in-depth overview of the market trends, emerging technologies, and how IQVIA eCOA is pioneering advancements in this space.
Medable Total Consent: The Future Of Informed Consent
With Total Consent, Medable is transforming the consenting process – harmonizing it into one simple-to-use platform that enables trial sponsors and CROs to completely customize eConsent.
Digital Versus Digitized: Common Misconceptions About eConsent
In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach.
eTMF Powered By AI: Automation Benefits And A Look At The Future
Watch the available webinar to find out solutions for how to continue to refine and improve eTMF’s ability to automatically classify documents.
Secrets To A Collaborative Model To Improve TMF Management
Speakers from Phlexglobal and Regeneron share the benefits of their highly effective partnering model and lessons learned that you can apply in your organization.
Notifications And Reminders
Configurable alarms appear as banner alerts on subjects’ devices, while email notifications help sites monitor potential non-compliance and respond to newly uploaded symptom severity data.
Trials And Tribulations Of Electronic Patient Consent: Removing Barriers To eConsent Adoption
After a decade of dabbling with eConsent, how can sponsors and technology providers meet the demand to bring clinical trials directly to the patient at a global scale? In this webinar, you’ll learn strategies to overcome the persistent challenges in eConsent adoptio...
Qualified eSignature in Electronic Consent Systems
This on‑demand session offers a clear, practical overview of the major eSignature types used in eConsent — ranging from simple electronic signatures to fully qualified electronic signatures — and explains when each is appropriate.
Enhancing Oncology Clinical Trials Through The Use Of Digital Technologies
The most difficult clinical research just became more challenging. Learn tactics on how teams can simplify oncology research while solving new and old issues.
The Rise Of The Site: Empowering Efficient Clinical Study Execution
Join the Co-CEO of CRIO, as he explores research site challenges and how site-based technologies can reduce administrative burdens, enhance efficiency, and eliminate redundant one-time-use technologies.
Central eSource: Leveraging Site Technology
In this presentation, CRIO founder and co-CEO Raymond Nomizu delves into how sponsors can leverage the electronic source trend among sites through the use of Central eSource.
Overview Of Central eSource From CRIO
Central eSource transforms the conduct of clinical trials by replacing disparate, site-specific source templates with a unified, sponsor-designed framework.
Right-Size Your eConsent Approach
Delve into the art of tailoring the eConsent experience to match your study and patients' specific needs, such as crafting eConsent documents, selecting appropriate delivery models, and more.
Eliminating Custom Functions From EDC
Watch this video to see how companies like ALCON are driving faster study builds and higher quality for complex studies with data-driven rules and dynamics.
The Medable Platform: Deep Evidence Generation
Discover how Medable's platform technology enabled a top vaccine developer to accelerate study deployment and recruitment timelines.
Elevating The Site Voice
A decentralized trial can be daunting for sites, but Medidata offers solutions to help site staff, sponsors, and patients move smoothly through the clinical trial process.
Innovations In IRT
Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials.
What It Really Takes To Adopt eConsent Across Large Pharma
Explore the benefits of incorporating consent management technology and discover practical strategies for developing effective change management and training programs.
Casebook Amendments In Vault EDC
Making casebook changes is easy in Vault CDMS, even in active studies. Use the simple, point-and-click interface to deploy changes to specific sites and subjects. Any new forms or fields are then flagged for site personnel to populate retrospectively for existing patients...
Defining And Implementing The Right Oncology Digital Strategy
A panel of oncology experts shares how top life science companies are using a combination of DHTs, ePROs, clinical trial platforms, and more to ease oncology research and drastically reduce timelines.
Introducing eCOA+ Streamlined Evidence Generation
Watch as Colin Weller, Vice President and General Manager of the Digital Outcomes and Evidence Platform at Medable, Inc., articulates the vision for eCOA+ and the trajectory of evidence generation.
Fast, Flexible, And Proven Direct-From-Patient Data Capture With eCOA
Delve into how IQVIA eCOA captures patient data in a way that always keeps patients top of mind.
Should Sponsors Provide Source Document Templates?
Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.
Closing The "Compliance Gap" In TMF Archiving
Discover how organizations are crossing this “compliance gap” with PhlexTMF for Viewing, an easily accessible TMF archive for internal use, audits, and inspections.
Selecting Medidata Rave: A Testimonial From Richmond Pharmacology
What made the Medidata's Rave EDC system stand out to Richmond Pharmacology during their vendor selection period?
eTMF Innovation
Watch the available video to see how AI-Powered Automation can streamline your Trial Master File Management.
Align eDiary Design With Assessment Schedules
Ensure alignment with your study protocol by leveraging the Sculptor portal to simulate eDiary completion and top-down scheduling, allowing for real-time preview and modifications.
IQVIA IRT - Putting The Focus On Driving Value For Our Customers
IQVIA IRT senior leader and expert, Dan Pavitt, highlights key IRT initiatives aimed at enhancing customer value in this Clinical Leader Solutions Expo presentation.
End-To-End Clinical Data Flow
Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.