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Tell Us What's Costing You the Most — We'll Fix That First

Whether it's deviation handling, batch records, or audit readiness — tell us the one thing keeping your QA team up at night. We'll show you how to get it live in weeks.

Start with One Module. Prove ROI. Then Expand.

We don't pitch 14 modules on the first call. Tell us about your compliance challenges — whether that's CAPA and deviation handling, batch records going digital, or regulatory response after a 483 — and we'll help you identify the right starting point. Live in 4–8 weeks, not 6–12 months.

"No lock-in, no pressure, no forced bundling — just a practical conversation about whether PharmaRegAI is the right fit for your plant."

Headquarters
United States of America
Response Time
Within 1 business day
FAQ

Quick Answers Before You Reach Out

Who should contact PharmaRegAI?

Any pharma manufacturer, CDMO, or contract lab — whether you have one plant or twenty — looking to get compliance and quality systems live without a year-long rollout. We built this for QA heads, plant heads, and VP Manufacturing — not IT departments.

Do we have to buy the whole platform?

No. You start with one module — usually CAPA/deviation handling, eBMR, or regulatory response — go live in 4–8 weeks, and expand only when the first module has proven ROI. No forced bundling.

How quickly can we get started?

We respond within 1 business day. After an initial 30-minute discovery call, we can scope your starting module within a week and have you live in 4–8 weeks — not 6–12 months.

What does a first conversation with PharmaRegAI look like?

A 30-minute call where we understand what's costing you the most right now — not a platform pitch. We'll identify the right starting module, give you an honest assessment of fit, and show you what "live in weeks" actually looks like for your plant.

Do you work with companies outside the US?

Yes. We work with pharma manufacturers globally — especially those subject to FDA regulations, EU GMP, or WHO-GMP standards. The platform is built for 21 CFR Part 11 and EU Annex 11 alignment from day one.