On-Demand Webinars
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Executing Decentralized Clinical Trials More Smoothly
11/17/2023
Seize the opportunity to elevate your approach to DCTs by watching this presentation on the importance of adopting a fully unified EDC/CDMS to alleviate the burdens on users, sites, and patients.
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Adopting Vault CDMS Accomplishments And Lessons Learned
8/31/2022
GSK leveraged an agile approach and modern ways of working to help shorten their EDC build times. Learn how they reduced EDC build and UAT times by 50% and had all new studies built within Vault CDMS in 18 months.
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Technology Overload: Addressing Site Challenges Of Digital Trials
5/23/2024
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.
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Using Remote Image Capture eCOA For Hybrid Dermatology Trials
2/1/2022
From eRecruitment, pre-screening, eConsent, and image-based data capture, explore how a decentralized trial design helps streamline enrollment, increase patient retention, and ensure data quality.
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Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations
2/22/2023
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.
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Improving Supply Chain: Accountability, Sustainability, Optimization
Watch as industry experts explore the advancements in drug accountability facilitated through IRT, encompassing innovative methods for managing site variations and sustainable supply chains.
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Top 10 Questions For Selecting The Best eTMF System
4/11/2022
An eTMF system can help Clinical Operations professionals manage the deluge of documents and data, but what capabilities are right for your situation? What is the best way to make the move to a modern eTMF from paper, spreadsheet trackers, or legacy tech to a new eTMF? Hear answers to these questions and more from a fellow Clinical Operations leader with experience in making the transition to an eTMF built for today's research ecosystems.
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Proven Practices For ePRO Adoption
12/8/2022
Industry experts discuss how a medical device company implemented ePRO to close gaps in data accuracy, reduce context switching for staff, and enhance patient convenience.
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Reinventing Prospective Study Data Acquisition And Delivery
7/23/2024
In a recent webinar, Sanofi and Flatiron Health leaders shared how a large academic medical center saved time and effort on trial data management using Flatiron Clinical Pipe™.
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No Code Requirement: Pre-Trial Insights For Operational Success
5/14/2024
Discover how a no-code solution transforms insight generation from weeks to minutes. Learn to run analyses, test hypotheses, and enhance patient trial recruitment and diversity with ease.