Today, clinical operations rely on a collection of point solutions that sit in silos and weren’t built to work together, creating redundancy and inefficiency. What if every element of your clinical trial could be managed through a single, unified platform?
mSource is Medrio's mobile eSource application that includes mPRO, mCapture, and mConsent. All products are native applications and are designed for use in early phase and Phase I research.
YPrime’s IRT+ goes beyond traditional IRT capabilities of patient randomization and drug supply management with control and a real-time view into critical functions and flows of a clinical trial - involving patient interactions, site activities and clinical supply management.
Communication and transparency are required to move a clinical trial forward efficiently, but how can you do this when you’re working with multiple external partners all using different systems with inconsistent reporting conventions?
ClinCard's Tax Toolkit supports research sites and sponsors in remaining IRS Tax compliant while maintaining confidentiality and privacy.
mCore is Medrio's all Phase eClinical suite which includes CloudEDC™. It is well suited for Phase II, III, IV, in Pharma, Diagnostics, Medical Device, and Animal Health studies.
New-generation IRT systems go beyond the fundamentals of randomization and drug supply to offer more functionality, visibility, flexibility and quality. Today’s advanced systems allow sponsors to fully control materials management, site and patient interactions, dosing scenarios, and treatment schedules down to individual patient and material unit levels. The IRT Worst Case Scenario Survival Handbook was built from YPrime’s knowledge gained, lessons learned, and creative solutions used to overcome study challenges and keep projects on track, no matter what.
Vault EDC provides a fast and intuitive interface for capturing and reviewing clinical trial data. Designed for flexibility, Vault EDC allows you to run complex multi-arm adaptive trials and make mid-study amendments without downtime or migrations. Veeva is delivering a better EDC that lets you run the trial you want.
Do you need to accelerate study cycle times, run the study you want, and get get clean data faster? Veeva Vault Clinical Data Management Suite offers EDC, data cleaning, coding, and review in a single unified suite.
Cenduit Drug Accountability Web-based tracking that closes the paper gaps.
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