Refine by
Locations
- USA
- Alabama
- Alaska
- Arizona
- Arkansas
- California
- Colorado
- Connecticut
- Delaware
- District Of Columbia
- Florida
- Georgia (Us)
- Hawaii
- Idaho
- Illinois
- Indiana
- Iowa
- Kansas
- Kentucky
- Louisiana
- Maine
- Maryland
- Massachusetts
- Michigan
- Minnesota
- Mississippi
- Missouri
- Montana
- Nebraska
- Nevada
- New Hampshire
- New Jersey
- New Mexico
- New York
- North Carolina
- North Dakota
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Vermont
- Virginia
- Washington
- West Virginia
- Wisconsin
- Wyoming
Site Investigation Software In Usa
4 software items found
by:Anju Software based inTempe, ARIZONA (USA)
RTSM Master delivers powerful randomization methods that, when combined with our fully validated and configurable trial modules, can perform robust subject screening and randomization, clinical supply management and investigational product assignments at designated drug dispensing visits. RTSM Master's randomization simulator can validate and support your testing and assumptions of ...
by:Medidata based inNew York, NEW YORK (USA)
Action Powered by Data and Advanced Analytics. Medidata is the only provider capable of taking 20+ years of data and insights and operationalizing it across the trial continuum, moving you beyond static, siloed systems, to an ecosystem providing a complete view of the patient and site experience, and unified workflows driving faster trial timelines. Medidata powers study teams with ...
by:Endpoint Clinical based inWakefield, MASSACHUSETTS (USA)
DRIVE: Clinical Supply Management Solution. An enterprise-level solution, DRIVE, enables you to manage clinical supplies at the sponsor, depot, and site levels, providing your team with full visibility and traceability of inventory across all trials, inclusive or exclusive of the use of an ...
by:ComplianceQuest (CQ) based inTampa, FLORIDA (USA)
A real-time view across clinical trial processes for higher-quality trial execution. Enable effective management of clinical trials with centralized data, transparent processes, and compliance with ...