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Medical Monitor Solutions

Get the details right to avoid controllable risks.

Key Takeaway

Proving efficacy and ensuring patient safety leaves little room for error among medical review teams. Saama removes the lag time between data requests and availability by eliminating manual work, removing data management complexity, and using machine learning to predict outcomes.

  • Easily see highlighted data changes 
  • Configure meaningful, patient-level insights
  • Gain real-time visibility into adverse events at the study, country, site, and patient level
  • Identify outliers, visualize trends, and gain access to actual test results
  • Impress your clients with your ability to reduce risk and keep clinical studies on track

Clinical Insights

See all safety and subject-level data together for consistent and proactive medical review. Innovative capabilities let medical review teams work at a higher level, to ensure patient safety and prevent studies from being pushed off course.

  • Access clean harmonized data from disparate sources—EDC, Labs, ECG, ePRO, IxRS, etc.—through a unified study data model
  • Customize KPIs and analytics for more relevant monitoring in real time
  • Set alerts to identify issues sooner for faster action
  • View data changes in real time, using dynamic line listings and graphical patient profiles
  • Use detailed labs, with access to actual test results, to visualize trends and identify outliers
  • Improve collaboration with key sponsor stakeholders, using custom dashboards and reports
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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.