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Clinical Intelligence Suite

Improve performance and reduce risk across your clinical trial portfolio.

Comprehend - Clinical Intelligence Suite

Everything You Need to Succeed

Comprehend’s cloud-based applications and services offer powerful data aggregation, monitoring, analytics, and collaboration capabilities, so sponsors and CROs can optimize study planning, enrollment, compliance, productivity, and oversight.

  • Reduce cycle times and improve data quality
  • Use real-time, actionable insights to keep studies on track
  • Integrate data from your preferred systems and use automatic alerts to identify and resolve issues before they become major problems`
 

ClinOps Insights

ClinOps VPs, study managers, CRA managers, and C-level executives all use ClinOps Insights to monitor study status and take action to avoid milestone delays.

  • Keep all your data clean and up to date, for optimal portfolio oversight
  • Quickly identify and address issues as they arise, from enrollment and compliance to site productivity
  • Drill down to root cause, to address issues and answer queries more effectively
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CRO Oversight & Collaboration

Sponsor study managers and vendor managers use this ClinOps Insights add-on to maximize CRO relationships and gain fast access to data that’s too often hidden from view. Real-time dashboards make it easy to track the performance of each CRO, study, site, and KPI.

  • Monitor CRO quality agreements and oversight plans in real time
  • Automate KPIs and thresholds to ensure compliance with ICH E6(R2) and other regulations
  • Resolve issues quickly with collaborative task management tools
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Centralized Monitoring

For sponsors and CROs alike, Comprehend’s Centralized Monitoring solution can be the cornerstone of an effective risk-based management strategy. Go beyond traditional site monitoring to significantly lower the cost, time, and risk associated with your clinical trial portfolio.

  • Allocate resources more effectively, using cross-study and cross-site KRIs, root-cause analysis, and configurable tools that adapt to evolving needs
  • Use automated alerts to reduce compliance risk
  • Reduce regulatory risk with fully auditable collaborative task management workflows
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Medical Insights

Medical Insights is the first application to bring all your safety and subject-level data into a unified structure, for consistent and proactive medical review and safety signal analysis. Chief medical officers, medical directors, data management professionals, and other stakeholders all use the innovative capabilities of Medical Insights to enhance the medical review process.

  • Use dynamic line listings and graphical patient profiles to highlight data changes
  • Address protocol deviations and adverse events earlier, to reduce risk and support patient safety
  • Use detailed labs, with access to actual test results, to visualize trends and identify outliers
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KPI Studio

Data management directors, medical directors, C-level executives, and quality control and compliance professionals benefit from KPI Studio’s ability to generate real-time dashboards based on the data points most relevant to each audience.

  • Use data from all your systems—EDC, ePRO, CTMS, IxRS, etc.—to create custom KPIs and analytics
  • Build meaningful tabular and visual reports
  • Enjoy better quality and ease of use through built-in syntax validation, advanced calculations, and formatting
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Access Out-of-the-Box Features in 4 Weeks—Guaranteed.

Saama can put you on the fast track to clinical trial process innovation.

Terms & Conditions

By inquiring about Saama’s Database Lock in a Day, you agree to be contacted by Saama and to allow Saama to use, maintain, store, and protect your personal data in accordance with our Privacy Policy.

Eligibility details are for informational purposes only. Saama, in its sole discretion, will determine your eligibility based on the information you disclose as part of the intake process. If Saama determines that you are eligible to participate, you will be notified by separate email. Eligibility depends on certain criteria, such as the size of your company, the types of clinical trials you sponsor, and the number of patients in–and stages of–your current clinical trials.

By completing the request form, you represent that you have authority to proceed on behalf of your company. Should you agree to participate, you agree to reasonably cooperate with Saama in following the guidelines and procedures required for integrating, standardizing, and analyzing your data. Participation requires the use of our Smart Data Quality application, a technology-agnostic AI engine that sits on top of your current infrastructure. The application can be used immediately, and you’re only charged for the services you use based on a predetermined estimate.

Information you share with Saama during your participation may be anonymized and/or aggregated, and made available publicly in Saama marketing materials. This information may include: types of systems and processes involved, types of departments involved, and size and regional location of your company. Such information will never be directly associated with you, nor will you or your company be identifiable without express written permission.