GxP compliant clinical trial analysis: Automated validation checks and streamlined workflows for accelerated regulatory submissions.

entimICE FastTrack in use

GxP compliant clinical trial analysis and reporting

Your profile

You are working with a pharma or biotech company with an active phase II/phase III clinical trial pipeline. Your clinical data science ecosystem is overly complex or outdated, in the worst case both. Your daily business processes are disconnected and inefficient and your clinical trial teams blocked by the inability to use the best tools for the tasks at hand.

Your challenge

Accelerating the timeline from database lock to submission is critically important for sponsors. However, in many cases, systems and processes are not well integrated, resulting in disruptions, delays, and disconnection of clinical data scientists from their tasks.

Our solution

entimICE FastTrack offers an open-platform clinical data repository and statistical computing environment.

It enables template-based study setups in just minutes and supports data ingestion pipelines from systems such as CTMS and EDC, as well as from data providers including CROs and laboratories.

Built-in study tracking and performance metrics keep managers informed and in control, driving faster submissions.

Automated checks and workflows streamline repetitive tasks, significantly accelerating the submission process.

Regulatory compliance is maintained automatically, ensuring consistent and reliable on-time submissions without the need for manual effort.

Take a closer look at the features and performance benefits we’ve developed to bring more speed and precision to every stage of your clinical trial services.

Explore entimICE FastTrack