E-TECHNOLOGIES
The Medable Platform: Deep Evidence Generation
Discover how Medable's platform technology enabled a top vaccine developer to accelerate study deployment and recruitment timelines.
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.
Is It Worth The Effort To Switch To Veeva's EDC?
Kronos Bio discusses how their oncology biotech switched to Vault EDC for faster, more flexible builds.
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.
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.
TMF Management In Clinical Trials
Elevate your knowledge of clinical trials and the Trial Master File by exploring three critical topics.
Document Processing: A New Hope
Tired of slow, error-prone document processing? Discover how top companies are boosting speed and accuracy while slashing costly rework. Watch now to learn how you can achieve TMF excellence faster.
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.
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.
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.
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.
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.
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.
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.
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.
Implementing Your eCOA For Optimal Clinical Trial Success
See how having the right tools to build intuitive and patient-friendly eCOA solutions can simplify the trial experience's inherent complexity, reduce participation burden, and drive engagement and compliance.
Smarter Trials Begin And End With Greenphire
Today’s clinical trials are more complicated and demanding than ever before. They’re often global, costly and require cumbersome travel. Greenphire is changing that. With our solutions, you can manage the entire financial lifecycle for trials conducted all ove...
BYOD Is Here To Stay
In this webinar, eCOA experts will explore how to implement a BYOD strategy, relevant BYOD regulatory considerations, and where the market is going from here.
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.
Rapid Study Design With The Sculptor Portal
Accelerate your eCOA assessment design with IQVIA eCOA Sculptor’s intuitive drag-and-drop interface, real-time feedback integration, and live simulations.
Rave RTSM: IRT Expo
Get an inside look at this RTSM solution, a full-service and unique platform-based approach to interactive response technology.
IQVIA eCOA: Amplifying The Patient's Voice
Dive deep into the capabilities of IQVIA's eCOA with our expert Edward Bartels. He will focus on how to effortlessly create a diary, schedule site/participant assessments, and intuitively manage translations and compliance.
Vault Safety-EDC Connection
Learn how to automate the flow of Serious Adverse Event (SAE) information between data management and safety systems, enabling more timely responses by Pharmacovigilance (PV) teams.
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.
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.
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.
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!
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.
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.
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.