E-Technologies STREAM
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Overcoming TMF Management Challenges For Small And Mid-Sized Companies
2/10/2021
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 adopting a fixed-fee, turnkey model encompassing everything required for ongoing TMF health, these organizations are achieving high-quality TMF compliance – with far less effort.
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Customer Testimonial – Chuck Bradley, Clinical Development & Operations Consultant
6/26/2024
In this testimonial, a Clinical Development & Operations Consultant highlights the industry-standard Medidata platform and the significant benefits of using a consistent system across sites.
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Deploy eConsent Around The World With Confidence
8/16/2022
Explore an easy, secure way to deliver highly engaging, regulatory-compliant electronic consent for trials of all types with IQVIA Complete Consent.
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Digital Versus Digitized: Common Misconceptions About eConsent
7/27/2022
In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach.
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Optimal eCOA For Vaccine Trials
8/23/2023
Delve into the pivotal role that technologies like electronic Patient-Reported Outcomes (ePRO) can play in generating substantiating evidence and streamlining vaccine trial operations.
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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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Do You Know Your TMF Health Score?
3/31/2022
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.
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The Diversity Imperative: EDC And Inclusive Clinical Trials
3/4/2024
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.
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Medable Total Consent: The Future Of Informed Consent
2/14/2023
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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Introducing eCOA+ Streamlined Evidence Generation
1/16/2024
Watch as Colin Weller, Vice President and General Manager of the Digital Outcomes and Evidence Platform at Medable, Inc., articulates the vision for eCOA+ and the trajectory of evidence generation.