E-TECHNOLOGIES
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.
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.
eTMF Innovation
Watch the available video to see how AI-Powered Automation can streamline your Trial Master File Management.
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?
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.
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.
Rethinking Today's ePRO Delivery For Tomorrow's Clinical Trials
Willie Muehlhausen, Co-CEO and Founder of Safira Clinical Research, and Tim Davis, VP of Strategy at MyVeeva for Patients, discuss how ePRO delivery needs to change to better serve modern trials.
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.
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.
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...
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.
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.
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.
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.
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.
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.
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.
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...
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.
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...
Unleash The Power Of IQVIA Complete Consent
Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.
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.
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.
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.
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.
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.
Rapid Study Design With The Sculptor Portal
Accelerate your eCOA assessment design to streamline UAT, mid-study updates, and protocol amendments effortlessly.
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.
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.
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.