Solutions
Mid-Market Pharma

Enterprise-Grade Quality. Without the Enterprise Price Tag.

GMP quality depth without enterprise complexity or cost. Built for mid-market pharma — typically $50M–$500M revenue across 2–5 sites, where VP Quality and IT buy together. Phase 1 GMP Core is in design-partner validation today.

The Challenge

What Teams Face Today

Mid-market pharma with multi-site GMP operations, caught between tools that don't scale and enterprise platforms that consume too many resources.

Enterprise Platform Cost

Legacy platforms priced for Fortune 500 pharma. Licensing, implementation, and maintenance exceed mid-market budgets.

Resource Constraints

Lean QA teams managing growing regulatory obligations across 2–5 GMP sites with manual processes and spreadsheet tracking.

Validation Burden

CSV and GAMP 5 documentation that consumes months of QA bandwidth before a platform is operational.

Scalability Gaps

Outgrowing point solutions but unable to justify full enterprise platform deployments.

How Verixa Helps

The Verixa Advantage

We bridge the gap — delivering enterprise-grade GMP quality in a platform priced and scoped for the mid-market.

Phase 1 GMP Core scoped for mid-market pharma running 2–5 sites — typically $50M–$500M revenue, with a VP Quality and IT as joint buyers. Currently in design-partner validation.

Right-Sized for Multi-Site GMP

Pricing

Right-Sized for the Mid-Market

United States

$110K–$350K ACV

Site-anchored, unlimited users in band. Confirmed post-design-partner validation.

India variant

₹30–150L + applicable GST

INR-denominated, site-anchored. Confirmed post-design-partner validation.

Ready to See Verixa in Action?

A focused walkthrough of Phase 1 GMP Core. 30 minutes. No obligations.