E-TECHNOLOGIES
Learn How ClinCard And ConneX Can Be Used For Your Next Clinical Trial
Sponsors, CROs and sites around the world partner with Greenphire to enable a secure and compliant electronic payment technology that makes their lives easier and removes the barriers to successful recruitment and retention. Watch this video to see how it works!
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.
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.
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.
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.
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.
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.
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...
Accelerate EDC Data Entry For Your Sites
Discover how you and your sites can benefit from Rave Companion, an easy-to-set-up and user-friendly tool that fits right into existing data entry workflows, ensuring simpler, quicker, and more accurate data entry.
Innovations In IRT
Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials.
Decentralized Clinical Trials In Action: Blending Clinical Payments Technology And eCOA For Study Success
When the catalyst of the COVID-19 pandemic wanes, we risk losing the progress our industry has made unless we collectively refuse to go back to the way things were before - and instead dedicate ourselves to implementing even more advancements and innovations that we'v...
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 ...
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?
Optimal eCOA For Vaccine Trials
Delve into the pivotal role that technologies like electronic Patient-Reported Outcomes (ePRO) can play in generating substantiating evidence and streamlining vaccine trial operations.
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.
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.
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.
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.
ConneX - Expert Travel Solution For Clinical Trial Participants
ConneX is the most comprehensive clinical trial travel solution designed to meet the unique needs of your global trials.
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.
Mastering Scientific Communication Plans Within Medical Affairs
Join industry leaders from Anju and 9 Labs for a presentation on the pivotal role of Strategic Communication Plans (SCP) in medical affairs.
Deploy eConsent Around The World With Confidence
Explore an easy, secure way to deliver highly engaging, regulatory-compliant electronic consent for trials of all types with IQVIA Complete Consent.
Customer Testimonial – Chuck Bradley, Clinical Development & Operations Consultant
In this testimonial, a Clinical Development & Operations Consultant highlights the industry-standard Medidata platform and the significant benefits of using a consistent system across sites.
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.
The Diversity Imperative: EDC And Inclusive Clinical Trials
In this EDC Showcase, experts delve into the crucial role of EDC in fostering diversity within clinical trials. Discover adaptable solutions for a more inclusive and efficient clinical workflow.
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.
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...
Verana Health Life Sciences: 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.
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.
Successful Subject Creation With eCOA, eConsent, & IRT Process Flow
Watch this process video to see how IQVIA’s integrated Interactive Response Technology (IRT) and electronic Clinical Outcome Assessment (eCOA) solution combined with unified platform delivery drives study orchestration and optimization.