Compliance
QMS & Compliance Platforms
ISO, FDA, and custom compliance management systems built for regulated manufacturing environments.
COMPLIANCE
QMS & Compliance Platforms
ISO, FDA, and custom compliance management systems built for regulated manufacturing environments.
The Challenge
Audit Season Should Not Be a Crisis.
Most manufacturers still manage compliance through spreadsheets, paper records, and institutional memory. When an audit arrives, teams spend weeks pulling data together rather than running production.
Paper-based records scattered across departments and shifts
Manual data entry from lab instruments introduces transcription errors
Audit preparation takes weeks — pulling teams away from production
Custom quality management software changes this. When every test result, calibration record, and approval is captured digitally at the source, audit readiness becomes continuous — not reactive
CAPABILITIES
Quality & Compliance Capabilities
Digital compliance that runs continuously — not just at audit time.
Document Control
Version-controlled SOPs, work instructions, and quality manuals with approval workflows.
Lab Instrument Integration
Direct data capture from testing instruments — eliminating manual transcription errors.
NABL / ISO Compliance
Audit-ready documentation for NABL, ISO 9001, ISO 17025, and industry-specific standards.
Batch Traceability
Full forward and backward traceability from raw material to finished product.
Calibration Management
Track instrument calibration schedules, certificates, and deviation handling.
Tamper-Proof Audit Trail
Complete audit trail for every data point, approval, and change — no gaps.
COMPLIANCE COVERAGE
Compliance Standards We Support
Designed to meet ISO, GMP, and industry-specific compliance requirements across regulated manufacturing environments.
NABL (ISO 17025)
Laboratory accreditation — test data management, calibration tracking, audit documentation.
ISO 9001
Quality management systems with process control, CAPA workflows, and audit readiness
ISO 22000 / FSSAI
Food safety management — HACCP plans, batch traceability, supplier qualification.
BIS / ISI
Bureau of Indian Standards compliance for manufacturing quality certification.
GMP / WHO-GMP
Pharma compliance with batch records, deviation tracking, and validation workflows
IATF 16949
Automotive quality — PPAP, APQP, control plans, and SPC.
FAQ
Common Questions
All records, approvals, and logs are digitally stored with full traceability, making audits faster and error-free.
Yes, the system is designed to support ISO, GMP, and industry-specific regulatory workflows.
Yes, it replaces paper-based processes with digital workflows and automated record keeping.
Yes, workflows are tailored to your SOPs, approval hierarchies, and audit requirements.
How We Work
Our QMS System Implementation Process
01
Discovery Sprint
2-week deep dive into your operations, systems, and constraints
02
Architecture
System design, data models, API contracts, infrastructure plan
03
Build Sprints
Two-week sprints with working demos every cycle
04
Launch & Scale
Production deployment, CI/CD, monitoring, ongoing support
Ready to Make Every Day Audit-Ready?
Start with a two-week Discovery Sprint. We map your compliance requirements, identify gaps, and design a system that turns audit prep from weeks to hours.
Svvatech
Production-grade software for manufacturing, logistics, and SaaS startups. Built in Chennai, deployed globally.
© 2025 Svavvashaa Technologies Pvt Ltd.
All rights reserved.
Get In Touch
- hello@svvatech.com
- Chennai, India
- +91 9XX XXX XXXX
Svavvashaa Technologies Pvt Ltd — CIN: UXXXXXXXXXXXXXXXXXXXXX
ISO-ready Engineering•India · US · UAE · APAC
Production-grade software for logistics,manufacturing,and SaaS startups. Built in Bengaluru, deployed globally.
© 2026 SVVATECH Pvt Ltd.
All rights reserved.
Services
Company
Get In Touch
sales@svvatech.com
(IN) +91-9980016879
#30/31, 1st floor, SRP Arcade, 6th block, 3rd Phase, Banashankari 3rd Stage, Banashankari, Bengaluru, Karnataka 560085