Pharma & Life Sciences
Audit-ready records, traceable batches and fewer late nights before inspections.
EIT Connect provides pharma software development for manufacturers, contract manufacturers, distributors and pharmacy chains. We build the systems quality, production and supply-chain teams depend on: electronic batch records, quality management, track-and-trace, pharmacy management and field-force apps. As a pharmaceutical software development company, we design every module with audit trails, access control and data integrity built in from day one, because in pharma, a record nobody can trust is as bad as no record at all.
What We Build
Our pharma software development services cover the full chain, from raw-material receipt and batch release to the distributor, the pharmacy shelf and the doctor's clinic. Most teams start where audits or stock losses hurt most, then add modules.
Digital batch manufacturing records with step-by-step instructions, in-process checks, weighing and dispensing, line clearance and review-by-exception. Batch release becomes a review of exceptions instead of a page-by-page hunt through paper.
Deviations, CAPA, change control, OOS investigations, complaints, document control and training records in one system, with workflows that route each record to the right reviewer and track it to closure.
GxP compliant software development means data integrity by design: secure audit trails, electronic signatures, role-based access and time-stamped records that follow ALCOA+ principles. We document requirements and testing so your validation team can qualify the system under your CSV approach, aligned with 21 CFR Part 11 and EU Annex 11 where they apply.
Unique codes for products and shipments, QR codes on API labels, aggregation from unit to carton to pallet, and scan-based verification at dispatch and receipt, so every pack can be traced back to its batch.
Our pharmacy management software development covers billing, batch and expiry control, prescription records, schedule-drug alerts, substitutes, purchase from distributors and near-expiry returns, for single pharmacies, chains and hospital pharmacies.
Pharma CRM development for sales teams: doctor and chemist masters, visit planning and reporting, sample and gift tracking, expense claims and territory performance, so managers see field activity daily, not at month-end.
Orders, schemes, free goods, credit limits and returns for C&F agents, stockists and distributors, plus temperature monitoring for cold-chain products in storage and transit.
Clinical trial software development for CROs and sponsors: site and patient management, visit scheduling, eCRF-style data capture, monitoring logs and trial documentation, with audit trails throughout.
Pharmacovigilance software development to capture adverse event reports from the field, call centres and literature, manage case processing and follow-ups, and prepare safety reporting for regulators.
Demand forecasting for production and distribution, expiry-risk alerts, field-force performance analytics and quality-trend dashboards that flag recurring deviations before an inspector does.
Who We Serve
A bulk-drug plant, a stockist and a pharmacy chain all deal with batches and expiry, but they need very different software. These are the six types of pharma businesses we build for.
Batch records, QMS, warehouse and line-clearance workflows for tablet, capsule, liquid and injectable plants preparing for CDSCO or export inspections.
Recipe and process control, solvent and yield tracking, QR-coded API labels and full lot genealogy from raw material to customer.
Client-wise batch records, tech-transfer documents, client portals for batch status and release, and costing by client and product.
Order management, scheme and free-goods calculation, batch-wise stock, near-expiry returns and credit control across hundreds of retailers.
Multi-store pharmacy management, central purchasing, prescription uploads, home delivery and customer refill reminders.
Trial management, site monitoring, sample tracking and research data platforms with controlled access and full audit history.
Apps
Field teams, warehouse staff and patients all need pharma data on a phone. Our pharma app development team builds iOS, Android and cross-platform apps that connect to the same validated back-end as your plant and distribution systems.
Doctor visit planning, call reporting, product presentations, sample distribution and expense entry, working offline in clinics with poor signal.
Typical features:
Goods receipt, batch-wise put-away, picking by FEFO, serialization scans and dispatch verification on handheld scanners.
Order medicines, upload prescriptions, get refill reminders and track deliveries, connected to pharmacy stock and billing.
Built native or with Flutter and React Native when one codebase for both platforms suits the budget.
Challenges
These are the issues pharma teams raise most often in our first conversations:
Slow reviews, transcription errors and missing signatures found the day before release.
Deviations, CAPAs and training records spread across files and spreadsheets.
Shared logins, no audit trail and edits nobody can explain.
Near-expiry stock found too late to return or sell.
MR activity reported weekly by WhatsApp or Excel, impossible to verify.
Customers and regulators asking for batch-level trace data the systems can't produce quickly.
Packaged pharma suites are expensive and rigid for mid-sized companies. Custom pharmaceutical software development gives you exactly the modules your SOPs need, at a cost that fits your scale.
Records, audit trails and approvals sit in one system, so preparing for an audit stops being a separate project.
Review-by-exception and digital checks cut the time between the last production step and release.
Batch-wise visibility from plant to pharmacy flags near-expiry stock while there's still time to act.
Daily, verified visit data shows which doctors are covered and where sales effort is going.
Workflows match your approved procedures, and you own the code with no per-user licence fees.
Technologies
Pharma software has to connect to lab instruments, ERPs, scanners and regulators' formats without breaking data integrity. We integrate with what you already run and build on a stack chosen for security and traceability.
PostgreSQL
MongoDB
AWS
Google Cloud
Docker 
Kubernetes How We Work
Regulated systems need traceable decisions from the first meeting. Our process produces the documentation your quality and validation teams expect.
We map SOPs, users, records and integrations, and write user requirements your QA team can review and approve.
Clickable screens for operators, reviewers and QA, plus a traceability matrix linking requirements to design.
Agile sprints with fortnightly demos, version control and documented testing for each requirement.
We provide test scripts and evidence to support your IQ/OQ/PQ, then pilot on one product line, warehouse or region.
Phased go-live, training records, monitoring and change-controlled updates under a support plan.
Timelines are typical planning ranges; validation scope and integrations can add time.
Why EIT Connect
Pharma software is judged by inspectors as much as by users. These are the commitments behind every system we build.
Audit trails, e-signatures and access control are part of the architecture, not features added after a finding.
Requirements, design and test evidence delivered in a form that supports your validation, not a pile of developer notes.
We configure workflows to your approved procedures and change them through your change-control process.
Full code and data ownership, cloud or on-premise hosting, and no per-user licences.
Encrypted data, role-based access, secure hosting and logged access, with personal data handled in line with India's Digital Personal Data Protection Act.
Pharma software development is building custom applications that help pharmaceutical companies manufacture, test, track, distribute and sell medicines in a compliant way. It covers electronic batch records, quality management, track-and-trace, pharmacy management, pharma CRM, clinical trial and pharmacovigilance software.
Our pharma software development services include electronic batch records, QMS, GxP-compliant software development, track-and-trace, pharmacy management, pharma CRM and MR apps, distribution and cold-chain tools, clinical trial software and pharmacovigilance software.
We build software with GxP requirements designed in, including audit trails, electronic signatures, access control and data integrity. Compliance itself is established when your organisation validates the system for its intended use, and we provide requirements, design and test documentation to support that validation.
Cost depends on the modules, number of sites, integrations and validation scope. A focused pharmacy, MR or distribution app costs far less than an eBR and QMS platform for a regulated plant. We share a fixed estimate after a discovery workshop.
A focused module such as pharmacy management or an MR app usually takes 3 to 4 months. A validated eBR or QMS rollout for a manufacturing site typically takes 6 to 12 months, including validation support and a pilot.
Yes. We integrate with SAP, LIMS, ERP and accounting systems so materials, batches and quality results stay consistent across systems, without manual re-entry.
Yes. Our pharmacy management software development covers billing, batch and expiry control, prescriptions, schedule-drug alerts, purchasing and returns for single pharmacies, chains and hospital pharmacies.
Look for experience with regulated workflows, data integrity by design, documentation that supports validation, integration skills and long-term support. At EIT Connect, you own your system, see working software every two weeks and work with one team from requirements to rollout.
Tell us where records, batches or stock slip through today: batch documentation, quality workflows, distribution or the field force. We'll show you what to build first, how it fits your SOPs and validation approach, and what it will cost.
Python
Node.js
React
Angular
Flutter
