Pharmaceuticals & Life Sciences

Web Application Development for Pharmaceuticals & Life Sciences

Web Application Development for pharmaceuticals & life sciences, built around the constraint that defines the sector: GxP validation means every system change needs documented evidence before it reaches production.

Regulations in scope
5
Systems we integrate
5
Typical first release
6 weeks

What changes when it is pharmaceuticals & life sciences

Accessibility is not a late-stage audit. Built in from the first component it costs almost nothing; retrofitted it costs a rewrite.

In pharmaceuticals & life sciences, GxP validation means every system change needs documented evidence before it reaches production. That single fact reshapes how web application development has to be built here, the guardrails, the approval points and the evidence trail are design inputs rather than things bolted on before go-live.

The workload we are most often asked to take on first is literature monitoring, usually integrated against LIMS. Integration comes before intelligence. A model that cannot reach your systems of record is a demo with good manners.

Built by engineers who ship production systems, not by a practice that subcontracts the build. You own the code, the models where they are open-weight, and the documentation to run it without us.

The sector constraints we design around

Defining constraint
GxP validation means every system change needs documented evidence before it reaches production
Regulations in scope
CDSCO · US FDA 21 CFR Part 11 · EU GMP Annex 11 · GxP validation · ICH guidelines
Systems of record
LIMS · QMS · eTMF · SAP · pharmacovigilance databases
Where we usually start
batch record review

Web Application Development workloads in pharmaceuticals & life sciences

  • batch record review
  • adverse event intake and coding
  • regulatory dossier assembly
  • deviation and CAPA drafting
  • literature monitoring

What is included

  • Architecture matched to your traffic and team
  • Core Web Vitals budget enforced in CI
  • Accessibility to WCAG AA
  • Authentication, roles and audit logging
  • AI features with streaming and graceful fallback
  • Deployment pipeline with preview environments

Questions from this sector

Can an AI system be GxP validated?

Yes, with a documented validation approach, IQ/OQ/PQ, defined intended use, change control and evidence of consistent performance. We build the validation pack alongside the system, not afterwards.

How do you handle 21 CFR Part 11?

Audit trails, electronic signatures, access control and record integrity designed in from the start, because retrofitting them is effectively a rebuild.

Which stack do you use?

Next.js with TypeScript and Postgres for most work, deployed on Vercel. We will happily work in your existing stack rather than insisting on ours.

Will it be fast?

We set an explicit Core Web Vitals budget and fail the build when a change breaches it. Performance regressions get caught in CI, not in production.

Can you take over an existing app?

Yes, starting with an audit of the codebase, dependencies and infrastructure before we commit to a plan.

Web Application Development for pharmaceuticals & life sciences, worth a conversation?

Tell us the workload and the regulation it sits under. We will tell you what is realistic.

Or email bd@dtrasglobal.com · call +91 74118 77878