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LSAC Business Apps

Operations Insights

Study managers, CRA managers, and C-level executives use Operations Insights to monitor study status and avoid milestone delays. By optimizing portfolio oversight, all your enrollment, compliance, and site productivity issues can be identified and resolved before becoming major problems. A fully auditable task management system facilitates collaboration, and an AI-powered virtual assistant provides instant answers to thousands of questions.

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Clinical Insights

Clinical Insights brings all your safety and subject-level data into a unified structure, for consistent and proactive medical review and safety signal analysis. Dynamic line listings and graphical patient profiles specifically highlight data changes for easier data management and faster resolution of protocol deviations and adverse events. What’s more, medical reviewers can use detailed labs—with access to actual test results—to visualize trends and identify outliers.

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Risk Based Quality Management (RBQM)

Using artificial intelligence (AI) and machine learning (ML), RBQM enables the continuous identification and mitigation of safety, efficacy, operational, study, and site risks throughout the design, conduct, evaluation, and reporting of your clinical trials. With the introduction of automatic risk assessment plans, anomaly detection, and advanced predictive KRIs, RBQM is your one-stop shop for risk management success.

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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.