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Industries

Built for teams where errors cost.

Deep experience where software meets regulation and real-world operations — and the same rigour for every other product we build.

Industries we serve

Pharmacovigilance, QA and regulated workflows that have to stand up in an inspection — not just a demo.

What we build
  • Drug-safety case systems
  • QA & document workflows
  • Validated web platforms
  • GxP
  • 21 CFR Part 11
  • EU Annex 11

LIMS and lab tools that follow every sample from registration to a signed, traceable report.

What we build
  • LIMS & sample tracking
  • Instrument integration
  • Patient report portals
  • NABL
  • ISO 15189
  • GAMP 5

Patient-facing apps and clinic tools that feel simple for patients and stay careful with their data.

What we build
  • Appointment & booking apps
  • Clinic dashboards
  • Care-team workflows
  • Mobile
  • Privacy by design
  • Integrations

From a first MVP to a multi-tenant platform — without a rewrite in between.

What we build
  • MVPs that can grow
  • Multi-tenant SaaS
  • Billing, admin & analytics
  • Next.js
  • PostgreSQL
  • Cloud

Ordering, tracking and operations tools that stay fast on the busiest day of the year.

What we build
  • Order & delivery tracking
  • Ops dashboards
  • AI support agents
  • Real-time
  • Mobile
  • AI agents
Up close

The problems we solve.

What tends to go wrong in each industry, and what we build to fix it.

Pharma & life sciences

01

Pharmacovigilance, QA and regulated workflows that have to stand up in an inspection — not just a demo.

What’s hard
  • Every change to a record has to be traceable and signed.
  • Inspectors ask for evidence, not promises.
  • Validation paperwork that takes longer than the build.
What we build
  • Drug-safety case systems
  • QA & document workflows
  • Validated web platforms
  • GxP
  • 21 CFR Part 11
  • EU Annex 11
GAMP 5 validation, explained

Diagnostic & QC labs

02

LIMS and lab tools that follow every sample from registration to a signed, traceable report.

What’s hard
  • Samples move across people, instruments and shifts.
  • Results retyped from instrument screens by hand.
  • Reports that must be reviewed, signed and traceable.
What we build
  • LIMS & sample tracking
  • Instrument integration
  • Patient report portals

Healthcare

03

Patient-facing apps and clinic tools that feel simple for patients and stay careful with their data.

What’s hard
  • Patients drop off when booking takes too many steps.
  • Clinic Wi-Fi that can’t be relied on.
  • Personal health data that has to stay protected.
What we build
  • Appointment & booking apps
  • Clinic dashboards
  • Care-team workflows
  • Mobile
  • Privacy by design
  • Integrations
Flutter vs native for business apps

SaaS & startups

04

From a first MVP to a multi-tenant platform — without a rewrite in between.

What’s hard
  • MVP code that can’t carry the next stage of growth.
  • Customer data that must never leak between tenants.
  • Billing, roles and admin work that eats the roadmap.
What we build
  • MVPs that can grow
  • Multi-tenant SaaS
  • Billing, admin & analytics
  • Next.js
  • PostgreSQL
  • Cloud

Retail & logistics

05

Ordering, tracking and operations tools that stay fast on the busiest day of the year.

What’s hard
  • Peak-day traffic that breaks slow systems.
  • “Where is my order?” questions all day long.
  • Operations data scattered across tools.
What we build
  • Order & delivery tracking
  • Ops dashboards
  • AI support agents
  • Real-time
  • Mobile
  • AI agents
AI agents for operations
Compliance

Standards we design for.

The regulations and frameworks our regulated and data-heavy builds are designed around.

21 CFR Part 11
US FDA — electronic records & signatures
EU Annex 11
EU GMP — computerised systems
GAMP 5
Risk-based computer system validation
ALCOA+
Data-integrity principles
ISO 15189
Medical laboratories — quality & competence
DPDP Act, 2023
India — digital personal data protection

We build the technical controls and the validation documents. Compliance itself also depends on your procedures, and validation sign-off stays with your QA team.

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