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Clinical Operations

Actionable insights reduce risk and improve study performance.

Key Benefits

ClinOps VPs, Study Managers, and CRA Managers are often frustrated by missing data and error-prone manual workflows. Saama solves these problems by automating oversight and collaboration across studies, systems, and CROs at every stage.

 

  • Enhance enrollment, compliance, and site productivity efforts
  • Save time and achieve milestones with automated alerts, which identify issues early so you can resolve them before they become major problems
  • Use an AI-powered virtual assistant to answer thousands of common questions instantly, without having to track down an expert
  • Quickly generate reports and deliver context-based insights to stakeholders via email or text
 

Operations Insights

Through a single operational portal, you can achieve comprehensive, real-time oversight of every study in your portfolio. Because data from your CTMS, EDC, ePRO, IxRS, and other systems is integrated and standardized into a unified study data model, you can quickly identify, visualize, analyze, and address issues early, before they cause major study delays. Automated alerts and task management tools make collaboration more responsive and efficient, and Saama’s AI-powered virtual assistant, known as DaLIA, provides instant answers to thousands of common operational questions.

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Risk Based Quality Management (RBQM)

Saama delivers an end-to-end solution that continuously engages users across the study lifecycle, from design and conduct to evaluation and reporting. With risk assessment plans, anomaly detection, automatic notifications, a collaborative tasking system, and built-in KRIs and QTLs, RBQM sets you up for success in managing and mitigating risk.

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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.