Software development for Pharma & Biotech

We've delivered multiple pharma & biotech projects addressing challenges like clinical trial data management complexity. We helped a biotech company cut clinical trial data entry time by 38% with a custom eCRF platform.

For pharma & biotech clients, we pay close attention to FDA 21 CFR Part 11 (US), GxP compliance, building these requirements into the architecture from day one rather than retrofitting them later. We'll confirm which specific regulations apply to your business during discovery.

The most common challenges we solve for pharma & biotech clients include clinical trial data management complexity and regulatory validation requirements for software systems. We tailor our discovery process to surface the specific version of these problems your business faces.

Yes, we build custom software tailored to pharma & biotech workflows rather than adapting generic templates. This typically results in better adoption and fewer workarounds than off-the-shelf alternatives.

Our engineers working on pharma & biotech projects stay current through ongoing client work, industry-specific research and ongoing dialogue with stakeholders in the space. This keeps our recommendations grounded in what's actually changing in pharma & biotech, not generic best practices.