E-TECHNOLOGIES
IQVIA eCOA Scribe Application
Experience seamless, secure, and flexible eCOA data collection with our application designed for diverse users, compatible with multiple devices, and equipped with offline functionality and robust authentication.
The Medable Platform: Deep Evidence Generation
Discover how Medable's platform technology enabled a top vaccine developer to accelerate study deployment and recruitment timelines.
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.
Impacting Sustainability Through Vendor Collaboration, Procurement
Guido D’Agostino, Head of Global Procurement at Chiesi, and Stefan Dürr, Senior Director of Product Management and Client Delivery at IQVIA IRT, delve into their achievements in sustainability.
The Journey From File To Trial: Automating Regulatory To TMF
In this webinar, we explore the value of automation between the Trial Master File (TMF) and Regulatory solutions. This connection can bridge the gap from the clinical trial to the regulatory filing, ensuring consistency of information while reducing duplicated data ...
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.
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...
TMF Management In Clinical Trials
Elevate your knowledge of clinical trials and the Trial Master File by exploring three critical topics.
Examining The "Why" And "How" Of Integrating Your eTMF And CTMS
As requirements for improved inspection readiness and quality risk management become more critical, discover the need to create a seamless integration and data flow between the eTMF and CTMS.
Agile eConsent: Taking A Flexible Approach To Global Implementation
Hear from industry experts on how they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.
The IQVIA Investigator Site Portal
Understand why companies are standardizing operations on a purpose-built, proven platform that empowers sites to succeed and provides sponsors with helpful insights.
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.
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.
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.
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.
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.
eTMF Innovation
Watch the available video to see how AI-Powered Automation can streamline your Trial Master File Management.
Technology Overload: Addressing Site Challenges Of Digital Trials
Watch as speakers explore the experiences of sites conducting digital and hybrid trials, discussing the critical benefits of a change management strategy and a unified digital trial platform.
Successful Subject Creation With eCOA, eConsent, & IRT Process Flow
Watch a short walkthrough of how IRT and electronic Clinical Outcome Assessment (eCOA) solution on a unified platform delivery drives smoother study orchestration.
Maximize Control And Transparency On The Path To Study Go-Live
Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.
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.
Crossing The TMF Compliance Gap With Inspection-Ready Access For Closed Studies
Your drug study is closed, you need inspection-ready access to the Trial Master File, but your CRO is ready to get the TMF out of their system and wants to send you a zip folder full of documents. What do you do? In this session, we explore an innovative new way to ensure...
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.
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.
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.
Preparing For 2022
2022 will be an important year for drug development. There are many questions around changes that came into play during the pandemic. A panel of experts look back over the year and into the future to help you prepare for the coming year.
Rapid Study Design With The Sculptor Portal
Accelerate your eCOA assessment design to streamline UAT, mid-study updates, and protocol amendments effortlessly.
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.
An AI Action Plan For The TMF Professional
Explore AI's impact on TMF processes in this on-demand webinar. Gain clarity on AI's potential, key evaluation criteria, and practical applications for enhancing TMF health and inspection-readiness.
Customer Testimonial – Keya Watkins, SVP, Oncology, Catalyst
Join Keya Watkins, SVP of Oncology at Catalyst, as she discusses the transformative impact of Rave EDC in enhancing competitiveness and sponsor engagement in oncology trials.