AI

AI-Powered Workflow

Accelerate your pharmacometrics processes with intelligent automation and AI-driven insights

DA

Data Analysis Planning

Create, edit, and manage comprehensive data analysis plans with ease

EX

NONMEM & PHIKL Execution

Execute scripts in NONMEM and our proprietary PHIKL software seamlessly

PM

Project Management

Manage project data, scripts, and execution from initiation to completion

RP

Report Writing

Streamlined report writing and management tools for professional documentation

CO

Team Collaboration

Built-in collaboration features for seamless teamwork and project coordination

PS

Poster Management

Create and manage scientific posters for conferences and presentations

SC

Script Management

Organize and version control your analysis scripts efficiently

SP

Speed & Efficiency

Dramatically reduce project timelines compared to traditional pharmacometrics processes

Automation & Scalability

Increase productivity and accelerate pharmacometrics analysis

DrLevy.AI fully automates pharmacometrics analysis from beginning to end, eliminating time-consuming manual steps and allowing you to concentrate on insights instead of endlessly navigating through settings. We help companies transition from scientist-operated pharmacometrics analysis to computer-automated pharmacometrics analysis.

We can launch at least 3,000 calculation engines per account, each capable of accommodating 500 unique profiles. This means 1.5 million PK profiles can be analyzed simultaneously in under 5 minutes!

The best part? The increase in productivity - When the time to run an analysis is reduced, each analyst can produce more work in the same time, lowering the cost of production significantly.

Data Cleaning & Custom Outputs

Clean smarter. Report faster.

DrLevy.AI gives you the power to transform raw pharmacometrics data into polished, ready-to-share results, all in minutes.

From BLQ handling and arithmetic conversions to custom tables, appendices, and plots, every step is streamlined and fully under your control.

The result? Efficient, flexible, and professional outputs that meet sponsor and regulatory requirements without extra manual work. Analysts spend less time fixing data and more time delivering insights.

Ready to Get Started?

Get a free demo and see our powerful features firsthand