Enterprise
Enterprise web platforms,
built to standards.
Audit-ready code, documented processes, and frameworks your procurement team already trusts. ISO 27001, SOC 2, GDPR, HIPAA, ISO 17025, FDA 21 CFR Part 11, WCAG 2.2.
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.
Information Security
Frameworks your CISO and procurement team already know.
ISO/IEC 27001
Information Security Management System (ISMS).
SOC 2 Type II
Service organization controls (security, availability, confidentiality, privacy).
ISO/IEC 27017 / 27018
Cloud security and protection of personally identifiable information in cloud services.
OWASP ASVS + Top 10
Application Security Verification Standard and the OWASP Top 10 vulnerabilities.
NIST Cybersecurity Framework
Identify, Protect, Detect, Respond, Recover.
Data Privacy
Privacy regulations that govern 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.
DPDP Act 2023
Digital Personal Data Protection Act, with consent management, data localisation, and Significant Data Fiduciary obligations.
HIPAA
US Protected Health Information rules for healthcare apps and any vendor handling PHI.
CCPA / CPRA
California Consumer Privacy Act and California Privacy Rights Act, with opt-out and deletion rights.
PIPEDA
Canada's Personal Information Protection and Electronic Documents Act.
Quality Management
Quality systems that auditors and accreditation bodies look for.
ISO 9001
Quality Management System, the universal QMS standard across industries.
ISO/IEC 17025
Competence of testing and calibration laboratories (paired with NABL accreditation locally).
ISO 13485
Quality Management System for medical devices.
CMMI
Capability Maturity Model Integration for software process maturity.
Industry-Specific Regulations
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.
EU MDR / IVDR
Medical Devices Regulation and In Vitro Diagnostic Regulation.
GxP
GMP, GLP, GCP, and GDP guidelines across the pharma value chain.
SOX (Sarbanes-Oxley)
Financial reporting controls and audit trail requirements.
PCI-DSS
Payment Card Industry Data Security Standard for any system that touches cardholder data.
IATF 16949
Automotive Quality Management System.
RBI / SEBI guidelines
Financial services regulations including data localisation and cyber-security mandates.
Accessibility
Public-sector and enterprise procurement increasingly require accessibility conformance.
WCAG 2.2 Level AA
Web Content Accessibility Guidelines, the global accessibility benchmark.
EN 301 549
EU accessibility standard for ICT products and services.
ADA Title III
Americans with Disabilities Act, applied to digital services.
Section 508
US federal accessibility requirements.
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
ISMS dashboards, control attestations, evidence repositories, and audit-trail systems aligned to ISO 27001, SOC 2, and similar frameworks.
Lab and quality management
Calibration, instrument records, sample workflows, deviations, CAPA, change control, and document control built around ISO 17025 and ISO 9001.
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 (CAIQ-style), 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
Are you certified to ISO 27001 or SOC 2?
We deliver to those standards but we are not formally certified as a studio. For engagements that require a certified vendor, we work alongside your existing 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, DPDP Act 2023, and similar regulations. We can also complete vendor security questionnaires, CAIQ assessments, and CIS Benchmark mapping 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. For DPDP Act 2023 sensitive data localisation, we keep data in approved locations 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.