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Data Management Team Solutions

Don’t let data issues delay your clinical trials.

Key Takeaway

As data becomes more voluminous and complex, mitigating data quality risk becomes increasingly difficult. Saama makes it easier for Data Managers to keep data clean and up to date, resolve queries faster, coordinate activities from start-up to database lock more efficiently, and make strategic contributions to risk-based monitoring (RBM) initiatives.


  • Unify and standardize data from disparate systems
  • Deliver real-time and predictive data analytics for greater visibility and faster identification of data quality issues
  • Quickly configure and distribute dashboards using the latest data

Operations Insights

Ensure sponsor success by tracking studies in real time and proactively identifying issues that could damage data quality or delay database lock.

  • Monitor every study across disparate data systems
  • Automate alerts to address data quality issues more quickly
  • Gain actionable insights to help mitigate risk
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Clinical Insights

With a central repository for safety and subject-level data owned by sponsors and CROs, Data Managers and medical review teams can avoid duplication and collaborate more effectively.

  • Focus on the most relevant data points
  • Automate alerts for better responsiveness to data quality issues
  • Easily move from an aggregate data view to a patient-specific view
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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.