Life Sciences Clinical

Saama Analytics’ AI-powered solution for Life Sciences offers clinical data management and analytics for clinical trial studies. The solution delivers harmonized and sanitized operational clinical data, prepped for analysis in order to draw business insights to make the clinical studies more cost-effective.
More than 80 percent of clinical studies fail to meet their timelines and budgets. With the AI capabilities of the solution, it is possible to minimize risks and streamline the study conducting processes. The solution works with study planning as well and helps with patient recruitment, site and PI selection, and protocol adherence.

Study Conduct

  • The Saama Analytics data engine pulls in data from disparate sources, such as CTMS, EDC, site data systems, and other systems of data records, and normalizes them.
  • The dashboard offers you a persona-based, and complete view of all aspects of your clinical studies. You get the ability to zoom in and out in dynamic views and drill down to any level to find out the source of any discrepancy.

Study Planning

  • Saama Analytics’ AI-enabled solution makes it possible to run multiple scenarios at the planning stage with various inclusion/exclusion criteria, allowing the most viable study plan to go into trial. Leveraging historical data and Real World Data (RWD), the Machine Learning (ML) algorithm of the solution helps you identify the most suitable patient pools and sets the right inclusion/exclusion criteria.
  • The solution takes into account various factors such as patient diagnosis, history of drug therapy, and any clinical procedures, to identify the relevant population groups by cross-referencing it with incidence rates and co-morbidities of the disease and many other target metrics.

Life Science Analytics Cloud

• Patient Registries
• Claims
• eTMF

Pre & Post Approval
Global Portfolio

Region, Country,
And Study-Based

Risk Management/

Site Performance

Data Quality &

• Site Performance
• Trial Performance
• Operations
• Physics
• Patient
• Investigator

• Lab
• Documents
• Biomarker
• Budget
• Supply Chain

Governance • Curation
Harmonization • Orchestration
Data Models • Clinical KPIs

• Safety
• Financial
• Resource Mgmt
• Trial Registry
• Site Registry




Key Benefits

The AI/ML solution delivers many significant benefits to the clinical study conduct and planning processes.

Global Clinical Portfolio Analysis during Pre- and Post-Approval Phases

Track and monitor the entire portfolio or focus on a single study and manage processes of drug development and commercial evidence generation to reach the market faster and with a more viable drug.

Operation and Financial Risk


Track the KPIs of the study to keep a constant check on real-time vs. planned outcomes to ensure any deviations are attended to and mitigated, and potential operational or financial risks are averted.

Milestone Management on the Basis of

Various Parameters

Monitor the status of the study on the basis of business strategy, region, country, or user persona by collating data from all available sources and harmonizing them to offer a single version of the truth.

Site Performance Management

Manage all clinical study data from sites to ensure performance expectations are met, and aspects like patient enrollment and retention are on track.

Data Quality and Compliance

Keep a check on the quality of recorded data, ensuring it has minimal errors so that it can be leveraged to deliver faster and more accurate insights.

Patient Recruitment

With machine learning capabilities you can design the most relevant inclusion/exclusion criteria to recruit eligible patients and minimize dropout rates.

Principal Investigator and Site Selection

Leverage historical data and past performances to select the most suitable PI and sites for a trial.