Key results
The company
Norstella
norstella.comData and advisory solutions for the pharmaceutical drug development lifecycle.
Result highlights
- Expected 1+ day savings per review cycle
The story
A pharmaceutical intelligence provider offering data solutions for market access, clinical trial matching, and commercial strategy to the biotech industry.
The risk evaluation process for commercial opportunities was entirely manual, requiring individual legal reviews that often took days to complete. This workflow created significant bottlenecks and led to inconsistent interpretations of compliance standards across submissions.
The organization utilized Replit to rapidly build an automated compliance application during an internal hackathon, moving from concept to working prototype in two days. The tool codifies regulatory logic directly into the workflow, ensuring submissions are evaluated against objective criteria rather than subjective review. This rapid development model allowed non-technical stakeholders to validate the solution immediately, bypassing traditional engineering delays.
Scope & timeline
- Prototype build time cut from weeks to 2 days
- Workflow creation cut from days to hours
Quotes
“Using Replit, we turned fragmented, reactive planning into proactive, data-driven engagement. Replit allowed me to easily create and demonstrate our vision to senior leadership during the hackathon with minimal disruption to our daily work. Going forward, this will reshape how I prototype data tools: faster validation, quicker pivots, and a more inclusive build process across non-technical stakeholders.”