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Check out this discussion from Clinical Leader Live on why many sites are still relying on paper-based systems and what "e" technologies are helping and increasing in adoption. |
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| 7 eCOA Design Recommendations: Insights From Sites And CRAs | Article | By Katie Garner, Signant Health | Signant joined a group of C-Path members including other eCOA solution providers, sponsors, and regulators for a GBTI project that revealed several opportunities to improve eCOA usability and flexibility. |
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| A Strategic Framework For Positive Site-Sponsor Relationships | Article | By Matthew Jones and Julia Scanlon, IQVIA Technologies | Through an examination of evolving trial strategies and implementation, we aim to lay the groundwork for a collaborative, mutually beneficial atmosphere, ultimately leading to a sustainable competitive edge. |
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| Earlier Disease Detection Study Utilizes EDC | Case Study | Castor | Understand how Optina Diagnostics streamlined operations and achieved significant milestones by leveraging Castor's tools in its effort to revolutionize the diagnostic process for Alzheimer’s. |
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| The Cutting Edge Of Pharma: AI And RWD | Webinar | Citeline | Taken from a spotlight session at the CNS Summit, gain insights from thought leaders from Norstella and Citeline regarding artificial intelligence and real-world data. |
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| Balancing Clinical Care With Digital Utility In Hybrid Trials | Article | By Dr. Graham Wylie, MRN - Medical Research Network | To create an effective decentralized clinical trial, tools and methods must be considered within the context of challenges faced by the clinical trial’s patients, physicians, and sites. |
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| How eConsent Can Help Legally Authorized Representatives | Article | Florence Healthcare | Software vendors often forget to think about the needs of LARs, even though they play a vital role in clinical trials. Explore three ways eConsent can help LARs complete the informed consent process. |
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