Solutions

Leading companies are seeing powerful results every day

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Trancelerate Digital Data Flow Overview Diagram

Enabling Digital Data Flow

Automate the creation of study metadata from standard configurations and system settings to support seamless clinical trial execution. This streamlined approach ensures that all necessary information is collected and organized efficiently, allowing researchers to focus on the trial's success.

70% or better mapping automation for generation of submission-ready SDTM data sets

Our solution integrates standards into the digital data flow at various touchpoints, ensuring continuity with existing workflows and processes. This means that you can easily incorporate new standards without disrupting your current operations or requiring significant changes to these processes

By incorporating standards into the digital data flow, we help reduce errors, increase efficiency, and improve overall data quality.

TLF Generation via Agentic AI

Tap into the power of Agentic AI without sacrificing the critical requirements for submission ready clinical trials. Our thought leadership in this solution is based on foundational ideas:

Human-in-the-Loop: Every AI-generated output is a "proposal" requiring human verification.

Auditability: Every command, prompt, and result is recorded in an immutable, compliant audit trail.

Reproducibility, end to end traceability atop a solution that works, not in weeks, not in days, but in minutes, for accurate TLFs from mock shells.

Sycamore Clinical Agentic Framework™ powers the first SCE CDR solution that comes with pre-validated AI Skills and scalable compute resources to achieve this automated and metadata-driven process..

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Statistical Programming & Data Sciences

The Sycamore CDR-SCE is a comprehensive solution for Statistical Programming, providing an interactive development environment, parallel processing, and collaboration tools to create, execute, and manage complex analyses.

Brought portfolio of companies into one environment

Choice of IDEs for programmers to use for writing, running, and debugging code. Collaboration among team members through shared workspaces and task management.

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Illustration of Real World Evidence

RWE with Regulatory Compliance

Our Real-World Evidence (RWE) solution streamlines the deployment of infrastructure for managing the Real-World data (RWD), its transformation and the analyses while ensuring trust and reliability through automated traceability. Within the platform, you can create a seamless flow of data, automate validation and review against regulatory standards, and ensure real-time visibility into data.

Reproducibility, end to end traceability with scalable storage and High Performance Computing

Administrators provide tools for exploratory analysis, data visualization, and analytics, while users write code in modern programming languages and create interactive apps. Built-in audit trails, task management, and lineage tracking ensure reproducibility and compliance, enabling high-quality decision-making and improved patient outcomes.

Smarter & easier

Managed deployment can be a superpower

Core, Professional, and Enterprise license packages can scale to meet the needs of any team

Packages deliver a selection of Modern Cloud Architecture, Computing Environment, Web Browser Access, Virtual Desktop Experiences, Automated Traceability / Dependency / Impact Analysis, Network Integrations, Active Directory Integrations, Services / Validation / Training / Support

  • Sycamore DSW provides access to our IDEs via the web, meaning we can write code, run, and schedule runs. Sycamore manages the servers and connects to the CDR, which controls access. It removes loads of extra work, and we never have to worry about the system going away of files getting deleted. It’s just a smarter deployment model.

    EXECUTIVE LEADER, GLOBAL MEGAPHARMA COMPANY

  • Hundreds of team members are able to use Sycamore because they simply spin up a container that includes R and code and data, with access control and auditing. It's easier than having our team manually installing their IDEs on servers.

    EXECUTIVE LEADER, GLOBAL PHARMA COMPANY

  • With this tool in place we envision that the protocol authors can view study build in the EDC within a day of changes in the protocol. ... This has been a fruitful endeavor as we made pragmatic decisions to optimize standards utilization by the many systems that rely on these standards.

    EXECUTIVE LEADER, GLOBAL PHARMA COMPANY

  • I just wanted to compliment the team [...], we have had a very successful first round of sprints in DEV and your team has been fantastic! Everything has gone smoothly and our Standards and Statistical programmers have had all their questions addressed, and feel well supported by the solution. We are looking forward to the next steps, but I wanted to relay my compliments so far.

    EXECUTIVE LEADER, GLOBAL PHARMA COMPANY

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