E-TECHNOLOGIES
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.
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...
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.
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.
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.
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.
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.
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>
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.
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.
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.
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.
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.
Castor eConsent: Site View
Study coordinators aim to enroll participants efficiently through a partnership that leverages direct-to-patient marketing to streamline recruitment.
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.
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.
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.
Game On! Strategies For Conquering The Final Boss: TMF Close-Out
Much like playing a lengthy and challenging video game, managing the TMF from set-up through close-out can be an epic journey. Ever wondered how to ensure you're well-prepared to face the final boss?
Reduce TMF Misfiles & Metadata Errors With Next-Gen AI-Enabled eTMF
Listen in as Chief Product Officer Jim Nichols, Product Manager Jim Horstmann, and VP Solutions Consulting Aaron Grant discuss issues and solutions for trial master files.
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...
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.
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 ...
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.
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.
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.
Functional Work Streams: Operationally Preparing Your Teams For Successful TMF Inspections
Inspection readiness is all about preparation. Not just having your documents in order, but also your team. In this session, seasoned TMF expert McKenzie Knudson will share a proven approach to getting your team ready for inspections.
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.
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.
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.