Take advantage of this checklist for evaluating eRegulatory solutions for clinical trial offices.
Zelta’s EDC has been used in more than 4,000 studies from startup to submission, across all phases, including over 500 phase 3c trials and 23 therapeutic areas.
Uncover how this unified platform is helping sponsors and CROs generate high-quality data, accelerate trials, and rapidly scale to Phase 2 and beyond.
Ease app localization challenges and communicate with your patients in their preferred language. Discover the benefits of translating and migrating eCOA with Applanga.
Legacy electronic Trial Master File (eTMF) systems are built on proprietary data standards or old file sharing tech. ArisGlobal is forging a new path.
Tackle CTMS by using this market report to help providers and sponsors better understand current trends surrounding this technology and be able to anticipate future ones.
Discover why more life science teams are using OpenClinica Unite™ to automate source data acquisition from patient medical record systems to clinical trial research databases and case report forms.
Clinical development organizations looking for efficient, expedient, and agile technology solutions should see how leveraging an eClinical suite with unified solutions and a single database can drive efficiency.
How you capture study data can make or break your organizational success, so why settle? Medrio’s EDC technology is intuitive, scalable, and proven across over 8,000 studies.
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Allow patients to share images and pictures from their own devices through Medidata’s eCOA without additional travel burden or disparate technology solutions.
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