E-Technologies STREAM
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Functional Work Streams: Operationally Preparing Your Teams For Successful TMF Inspections
7/14/2021
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.
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eTMF Innovation
8/25/2021
Watch the available video to see how AI-Powered Automation can streamline your Trial Master File Management.
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Trials And Tribulations Of Electronic Patient Consent: Removing Barriers To eConsent Adoption
6/3/2021
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 adoption and gain the benefits promised from successful decentralized trials with remote capabilities for patients and sites.
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Rethinking Today's ePRO Delivery For Tomorrow's Clinical Trials
6/24/2024
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.
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Customer Testimonial – From CRA To Management
6/26/2024
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.
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Vault Safety-EDC Connection
6/24/2024
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.
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Examining The "Why" And "How" Of Integrating Your eTMF And CTMS
6/24/2022
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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Veeva eCOA Demo
6/24/2024
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.
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The Art Of Accelerated Study Closeout: End Of Study Solutions
11/2/2023
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.
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What It Really Takes To Adopt eConsent Across Large Pharma
3/27/2024
Explore the benefits of incorporating consent management technology and discover practical strategies for developing effective change management and training programs.