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Work smarter with your preferred tools and draw more informed conclusions.

Key Benefits

Defining Statistical Analysis Plans (SAP) and providing statistical support to clinical studies requires access to complete, accurate, and up-to-date data from a variety of sources. Saama makes it easier to compare data across patients, sites, and studies so you can track and resolve deviations from the SAP.

  • Eliminate manual work through automatic data change highlighting
  • Quickly identify adverse events at the study, country, site, and patient level
  • Gain a fuller picture of your cohorts through the ability to visualize trends, identify outliers, and access actual test results

Smart Programming and Analysis Computing Environment (SPACE)

Gain the flexibility to use your preferred editing tools for more efficient and effective collaboration in a secure and validated environment. Simplify study setup, process implementation, and job management for both exploratory analysis and regulatory submission.

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Active Safety Analytics for Pharma (ASAP)

Use real-world data (RWD)—healthcare claims and electronic medical records (EMR)—to find associations between any drug in the marketplace and patient outcomes. Just like the FDA’s Sentinel Initiative, ASAP leverages an advanced statistical (TreeSCan) methodology to unlock specific safety signals from billions of records in the health profiles of millions of patients.

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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.