E-TECHNOLOGIES
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.
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.
eTMF Innovation
Watch the available video to see how AI-Powered Automation can streamline your Trial Master File Management.
Innovations In IRT
Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials.
Veeva eCOA Demo
See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.
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.
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.
TMF Completeness: Simple Solutions For A Complex Problem
In this session, two of the top technology minds in TMF management will demonstrate and a simple yet innovative way to measure completeness at any point during the trial.
Do You Know Your TMF Health Score?
For inspection-readiness, the critical attributes of TMF health are completeness, timeliness, and quality. View our experts explore what your TMF Health Score could be and how this can be used to achieve and maintain ongoing TMF health and inspection readiness.
Selecting And Expanding Your EDC System: A Testimonial From Everest Clinical Research
Everest Clinical Research shares what lead them to strengthen their partnership with Medidata, and expand past the use of Medidata's EDC products too other helpful solutions.
Introducing A Smarter, More Cost-Effective Way To Run Clinical Trials
While early-phase trials often rely on less capable, cost-effective systems, the transition to more complex studies in later phases necessitates a more robust EDC system.
Auto Generate Documentation
Unlock seamless software development with IQVIA’s eCOA, which automates screenshots, validation documentation, and audit trails, ensuring real-time updates, easy exports, and full traceability.
Addressing Site And Sponsor Challenges In Digital Trials
<p>While the digital transformation of clinical trials has made tremendous strides in recent years, the plethora of new technologies can overwhelm. Learn how to help sites and sponsors combat the overload of technology.</p>
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...
Rapid Study Design With The Sculptor Portal
Accelerate your eCOA assessment design to streamline UAT, mid-study updates, and protocol amendments effortlessly.
Overcoming TMF Management Challenges For Small And Mid-Sized Companies
Maintaining an inspection-ready Trial Master File is becoming increasingly burdensome, even for teams with significant resources. In this webinar our experts walk through a new, full-service TMF management approach implemented by smaller biopharmaceutical companies. By ad...
Study Build And Scheduler Tools
Empower your study participants with IQVIA eCOA’s tailored user experiences, flexible event triggers for clinicians, comprehensive training resources, and 24/7 support for seamless study management.
An Honest Assessment Of eCOAs From A Site Perspective
Listen to what sites have to say about the changing nature of COAs in clinical trials, including the usage of eCOA, its benefits, and ways to improve the technology.
Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations
Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.
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.
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 ...
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.
Harness The Power Of eCOA In Your Next Trial
In this webinar, explore the importance of eCOAs, how they have evolved from the standard paper diaries, and what efficiencies you can realize from them.
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.
Rave RTSM: IRT Expo
Get an inside look at this RTSM solution, a full-service and unique platform-based approach to interactive response technology.
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.
Electronic Data Capture Solutions For Your Phase I and Phase IV Studies
Take a cost-effective approach to meet your study's data capture, management, and analysis needs with a solution customized to your clinical trial.
Customer Testimonial – From CRA To Management
Join Brittany Erlandson, Sr. Manager of Clinical Operations at QuidelOrtho, as she shares her journey from CRA to management and the crucial role of Medidata's EDC system in enhancing efficiency.
Seamless And Integrated Onboarding For Trial Participants
Streamline your patient experience with a comprehensive, all-in-one solution that allows you to recruit, screen, and enroll participants remotely from the comfort of their own homes.
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...