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Operations Insights

In just four weeks from the time of data access, Saama can make Operations Insights your single portal for day-to-day clinical operations.

An intuitive interface enables ClinOps VPs, study managers, CRA managers, data managers, and other stakeholders to quickly find and analyze the data they need to gain insights and take effective action.

Saama’s revolutionary Deep Learning Intelligent Assistant (DaLIA) lets users “converse” with data for immediate answers to thousands of common questions, without having to track down a subject matter expert.

LSAC: Operations Insights

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  • EDC
  • CTMS
  • eTMF
  • Financial
  • Resource Mgmt
  • IRT/IVRS RTSM
  • Site Performance
  • Trial Performance
  • Operations
  • Investigation
  • Biomarker

Governance • Curation • Harmonization Orchestration • Unified Data Model • Metrics Ad-Hoc Reporting • Conversational UX

 

Portfolio Analysis

At-a-glance dashboards show status and progress for a single study or your entire portfolio. Predict delays with cross-study comparative forecasts, answer questions about risk areas, and determine resource allocation and investment needs.

 

Milestone Management

Saama makes it easy for regional, country, and study leaders to manage sites and studies from a single source of truth. Automated alerts identify issues early, so you can take corrective action that prevents delays and avoids cost overruns.

Solution Brief
 

Study and Site Performance

End-to-end visibility, prebuilt KPIs, and real-time data aggregation take the guesswork out of identifying at-risk sites and resolving issues before they become major problems.

 

Data Quality and Compliance

With complete data visibility and AI-powered predictive capabilities, it’s easier than ever to identify root causes and prevent errors.

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.