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By Aurea M. Flores, Ph.D. | Consultant Aurea Flores, Ph.D. summarizes some of the clinical trial technologies used by clinical research sites, their capabilities, and how sponsors and sites might best evaluate their use in clinical research. |
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| Evaluating EDC Systems In A Modern DM Landscape | Article | Veeva Systems, Inc. | This guide provides five crucial recommendations to refine evaluation strategies and choose the right solution for today's complex clinical data environment, optimizing data collection practices. |
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| How eConsent Delivers Value For Sponsors | Article | By Vinita Navadgi, IQVIA Technologies | Delve into the data substantiating experiences with electronic informed consent to better understand their positive impact on the outcomes of clinical trials. |
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| Are We Ready For A Unified Clinical Platform? | Webinar | Cognizant | Industry experts share their perspectives on end-to-end clinical development, essential elements of a unified clinical platform, as well as the associated benefits and challenges involved. |
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| Introducing Digitally-Enabled Biosample Consent Storage | Article | Medable | Despite the rise of digital solutions in healthcare, paper consent forms are still common in today’s clinical trials. Unfortunately, these paper forms pose significant challenges in retaining the documentation. |
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