CTOS_Datasheet_23.09.24

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Clinical Trials Oversight System (CTOS)

Get clinical insights that drive real results with unified clinical, operational, and real-world data

Why Choose CTOS?

CTOS is a flexible platform designed to help complex clinical trials—traditional site-based, decentralized, hybrid, or 100% virtual. Using advanced automation, CTOS brings greater visibility to your trial data at both the study and portfolio levels.

Benefits

Integrate and automate the data-to-analytics process to mitigate risks, save time and avoid expensive delays, errors, and bottlenecks.

Gain continuous oversight at study and portfolio levels, standardizing data ingestion from disparate systems and sources for easier analysis and reporting.

Ensure patient safety and trial integrity with data-driven oversight, powered by a preconfigured library of hundreds of metrics for spot-on monitoring.

Get real-time acces to a single-source-of-truth data repository to meet important milestones.

Keep studies on track with alerts, role-based controls, version controls, and interactive dashboards.

Clinical Trials Oversight System (CTOS)

Key features

Source Agnostic

Accepts data from 40+ systems across clinical operations and patient data sources.

Decentralized

Unlocks potential for decentralized trials with real-time data aggregation and transmission and rapid error identification.

Automated

Automates data ingestion, cleaning, and standardization, reducing data delivery time from weeks to hours. Preconfigured quality checks and updated dashboards make the user experienced seamless.

Single Source of Truth

Acts as a Clinical Data Repository housing the most current and precise version of the data, thereby preventing data duplication and optimizes storage resources. This is based out of a Common Data Model (CDM) created for supporting various business needs includes Visualizing Data for decision making, biometrics statistical analysis, reporting and exporting.

Monitor trial activity between sponsor, CRO and other partner systems.

About MaxisIT

MaxisIT’s purpose-fit and intelligent clinical data analytics platform helps improve clinical trial performance, mitigate risk, and optimize clinical outcomes. We provide a centralized and reliable source of truth for diverse data types from various sources, giving life sciences companies real-time insight to shorten cycle time and increase return on investment. Incorporating an end-to-end clinical data pipeline from intake to visualization, MaxisIT's solutions are powered by AI/ML and metadata-centric approaches. Our impressive portfolio of over 3,300 clinical trials and an unparalleled 100% customer retention rate affirm the quality and reliability of our services.

“Having the highest quality clinical data and related information with efficient analytical tools available at all times is critical to managing our clinical programs and accelerating our innovation; and with MaxisIT’s Integrated Clinical Development Cloud, it was easy to achieve that across the portfolio of studies, and we were able to improve the quality of data and speed of decisions without increasing our support staff.”

Head of Clinical Projects

A multi-billion pharmaceutical company

https://maxisit.com/

510 Thornall Street, Suite 180, Edison, NJ 08837

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