Enterprise
Enterprise web platforms,
built to standards.
Audit-ready code, documented processes, and standards we have actually delivered against. GDPR, ISO/IEC 17025 with NABL, FDA 21 CFR Part 11, and GxP (GMP, GLP, GCP).
Standards and frameworks
The frameworks we build to.
We are not a certified body. We deliver to the same control frameworks your auditors and procurement team already use. Documentation, audit trails, and process artefacts come standard.
Quality and Laboratory
Lab competence and quality systems that auditors and accreditation bodies look for. Proven on past lab software.
ISO/IEC 17025
Competence of testing and calibration laboratories. Past work: Calforms, BIS Data Assistant, QMS Total.
NABL accreditation support
Records, traceability, and audit checklists structured to support NABL assessments locally.
Life Sciences and Pharma
Sector-specific rules that change what your software must prove and log.
FDA 21 CFR Part 11
Electronic records and electronic signatures for pharma and life sciences. Past work: Kemwell, BIS Data Assistant.
GxP (GMP, GLP, GCP)
Good practice guidelines across the pharma value chain. Past work: lab data systems for pharma QA teams.
Data Privacy
Privacy regulation that governs how customer and employee data is collected, stored, and shared.
GDPR
EU General Data Protection Regulation, including data subject rights, lawful bases, and cross-border transfer rules. DPA signed on request.
How we develop
The way we build is the compliance.
We do not bolt audit-readiness on at the end. It is in how we scope, prototype, build, and hand over every regulated project.
Prototype before code
You approve a wireframe or working prototype before we build a single screen. No surprises at delivery.
Live previews from day one
A preview link from the first day. Watch the build come together and request changes while they are cheap to make.
Audit trails by design
Every action logged, made immutable where the standard requires it, with electronic records and signatures built in.
Validated and documented
Method validation logs, equipment records, and validation documentation produced on request for your audit team.
Region-pinned deployment
Data stays in the location your audit and compliance team requires, with the architecture documented.
Owned by you
Full source code, documentation, and access on handover. No vendor lock-in, ever.
Enterprise clients
Trusted in regulated and audit-heavy environments.
Bureau of Indian Standards
Tamper-proof gold measurement system. Insert-only database. Government-grade audit integrity. In daily use at BIS facilities. Three follow-on desktop applications commissioned after the first.
Kemwell Biopharma
RADWAG Multi Connect for pharmaceutical manufacturing. Multi-instrument data collection across lab balances, feeding a single audit-ready database for batch certification.
LCGC
Lab data assistant and QMS platform. Excel-like desktop application for analytical chemistry teams to record, filter, sort, and merge lab data with full audit trails.
QMS Total
Quality management platform spanning calibration, lab management, deviations, CAPA, and document control. The umbrella under which CalForms, RNexus, LabZ, and TruGold live.
Software we built
Products shipped under qmstotal.com.
Quality, calibration, and lab management software built and maintained for regulated industries over the past decade.
ISO 17025 Compliance Software
Audit-ready compliance platform for testing and calibration laboratories.
Document control, equipment records, method validation logs, internal audits, and corrective actions. Built to align with ISO/IEC 17025 and NABL audit checklists.
Calforms
Calibration management software for metrology and quality teams.
Calibration scheduling, instrument records, traceability, certificate generation, and out-of-tolerance workflows. Used inside lab and manufacturing QMS environments.
RNexus
Research and quality nexus for enterprise QA teams.
Cross-functional research and quality data hub built under the qmstotal.com umbrella for regulated environments.
LabZ
Lab management system for sample, test, and report workflows.
Sample lifecycle, test instrument integration, observation entry, reviewer-approver workflows, and report generation.
TruGold
Specialist assaying and quality platform.
Vertical software for precious-metals assaying, with traceability, custody chain, and certificate workflows.
What we build
Capabilities for regulated and audit-heavy work.
Compliance and audit software
Control attestations, evidence repositories, document control, and audit-trail systems for your internal quality and compliance program.
Lab and quality management
Calibration, instrument records, sample workflows, deviations, CAPA, change control, and document control built around ISO/IEC 17025 and NABL.
Pharma and life-sciences platforms
Validated systems with electronic records and signatures (21 CFR Part 11), audit trail integrity, and GxP-aligned change control.
Customer portals and dashboards
B2B customer portals, partner consoles, distributor dashboards, and white-label embeds with role-based access and SSO/SAML.
Document and content management
Versioned document libraries with workflow approvals, e-signatures, retention policies, and full audit trails.
AI integration in regulated environments
LLM-powered features (search, extraction, copilot) with prompt logging, model evaluation, human-in-the-loop review, and PII redaction.
How we deliver
Procurement-friendly by default.
Every enterprise engagement comes with the artefacts your audit, security, and procurement teams expect.
Mutual NDA before scoping
Standard mutual NDA signed before we discuss scope, architecture, or sample data. Available in your preferred template.
Documented scope and milestones
Every engagement starts with a written scope, deliverables list, milestone schedule, and acceptance criteria. Procurement-friendly format.
Security review checkpoints
Architecture review, data flow diagrams, and threat modelling sessions during design. Pen-test-ready handoff if your security team requires it.
Audit-ready repository
GitHub with branch protection, signed commits, CODEOWNERS, mandatory reviews, dependency scans, and SBOM exports on request.
Compliance documentation pack
Architecture doc, data residency statement, vendor security questionnaire, DPA, and processor agreement on request.
Handover with knowledge transfer
Code walkthrough on Loom, runbooks, on-call procedures if applicable, and 30 to 90 days of post-launch support depending on the engagement.
Procurement questions
Which compliance standards have you delivered against?
We deliver to GDPR, ISO/IEC 17025 with NABL, FDA 21 CFR Part 11, and GxP (GMP, GLP, GCP). These are standards we have actually shipped software for, not a generic list. We are not a certified body, so for engagements that require a certified vendor we work alongside your certified hosting and infrastructure providers (Vercel, AWS, Azure) and document our processes against the same control framework.
Can you sign a Data Processing Agreement (DPA)?
Yes. We sign DPAs for GDPR and similar regulations, and we complete vendor security questionnaires on request.
How do you handle data residency requirements?
We deploy to the region you specify. Vercel, AWS, Azure, and Supabase all support region pinning. We keep data in the approved location and document the architecture for your audit team.
Do you do penetration testing?
We make code pen-test-ready. Most clients run pen tests with their preferred third-party (Crowdstrike, Bishop Fox, NCC Group, regional firms). We then remediate findings as a fixed-scope engagement.
What is your typical enterprise pricing?
Enterprise engagements are scoped per project. Builds typically start at ₹2,50,000 with NDA, scope doc, milestone schedule, and acceptance criteria. Smaller enterprise websites that fit our standard packages can use the listed pricing.
Can you work alongside our internal IT team?
Yes. We deliver code your team owns, with full documentation, runbooks, and a handover checkpoint. We also offer Hire a Techie retainers if you want ongoing developer capacity inside your stack.
Bring us your RFP.
Mutual NDA on day one. Scope doc and milestone schedule on day two. Working software soon after.