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E-TECHNOLOGIES

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The Art Of Accelerated Study Closeout: End Of Study Solutions

Watch as experts from eClinical Solutions and Medidata delve into end-of-study process challenges, the transition to electronic distribution and management, the advantages of leveraging a digital platform, and more.

2:35 Checklist
Get Your TMF Health Score

Introducing the TMF Health Score – an expert methodology that provides an “early warning system” to commonly overlooked issues that often lead to inspection findings.

56:44 Phlex
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...

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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.

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.

56:13 Actigraph Modernizing Clinical Research
Modernizing Clinical Research With AI And Digital Data

Discover how ActiGraph is revolutionizing clinical trials with patient-focused digital data and cutting-edge technology that enhances trial efficiency across all phases.

2:22 medable total consent video
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.

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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.

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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.

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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.

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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.

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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.

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Innovations In IRT

Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials.

1:28 Overview of Central eSource From CRIO
Overview Of Central eSource From CRIO

Central eSource transforms the conduct of clinical trials by replacing disparate, site-specific source templates with a unified, sponsor-designed framework.

38:24 Medidata EDC
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.

3:31 Elevating the site voice
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.

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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.

31:39 At The Crossroads Of Data
At The Crossroads Of Data: eCOA And Sensors Converging For Novel Insights

Leveraging sensors and eCOA addresses increasing clinical trial complexity and ensures a more efficient and effective study design.

1:43 IQVIA eCOA Localization
Streamlining Translations For Global Studies

Ensure seamless, accurate global study translations and efficient localization with IQVIA eCOA, leveraging our proven vendor relationships and streamlined process to keep your study on track.

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The Medable Platform: Deep Evidence Generation

Discover how Medable's platform technology enabled a top vaccine developer to accelerate study deployment and recruitment timelines.

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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.

1:54 IQVIA eCOA Sculptor Portal
Real-Time Data Tracking And Compliance Monitoring

Unlock real-time data tracking, customizable reporting, and proactive compliance monitoring with the IQVIA eCOA Sculptor Portal to enhance clinical decision-making and ensure protocol adherence.

2:19 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.

2:40 phlexglobal tmf video
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.

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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.

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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.

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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.

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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>

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Building One Home for Sites

Watch this presentation and demonstration of One Home for Sites for the latest updates on how the industry is coming together — even competitors — to alleviate the technology burden on research sites.