
CPD technology solutions empowers accredited laboratories and compliance-driven organizations with integrated digital solutions for quality management, accreditation readiness, and regulatory excellence. From LIMS to audit management—everything you need as modular platform. Trusted by 50+ ISO Accredited organizations across India and Nepal.





















CPD’s modular Technology platforms addresses the three pillars of compliance: Intelligent Operations, Secure Reporting, and Governance Excellence.
Laboratory Information Management System (LIMS)
Centralized platform for sample-to-report management with full traceability. Eliminates spreadsheets, reduces errors, and ensures ISO/IEC 17025. Perfect for labs, testing facilities, and quality-driven organizations.
Magical QR & Report / Certificate Verification
Secure QR-based system for instant lab report verification. Build stakeholder trust, eliminate fake reports, and meet ISO 17025 Accreditation like NABL requirements.
20,000+ codes generated, 15,000+reports verified, zero fraud incidents and growing.
Document Management System (DMS)
CPD DMS centralises and streamlines all document control processes, including SOP management, policy control, version tracking, approval workflows, and comprehensive audit trail maintenance.
It enables laboratories, inspection bodies, and ISO-certified organizations to efficiently manage controlled documents while ensuring full compliance with ISO 17025, ISO 15189, ISO 9001, and ISO 27001 standards.
Since 2015, CPD Technologies has been the trusted compliance infrastructure partner for accredited laboratories, healthcare facilities, manufacturing organizations, and government agencies. We understand the unique challenges of maintaining ISO compliance, NABL accreditation, and quality management at scale.
ISO 9001:2015 & ISO/IEC 27001:2022 Certified
Empowering accredited laboratories and compliance-driven organizations with integrated digital solutions for quality management accreditation readiness, and regulatory excellence.
To be the leading compliance infrastructure partner for
ISO-oriented organizations globally, enabling digital-first
quality management and regulatory excellence.
Solve your compliance fast, so you can focus on what matters—testing excellence. From day one, we’ve built our reputation on speed, clarity, and proven results in accredited lab environments.
Backed by team working in Compliance based technology development from 2010
ISO 27001:2022 certified with AES encryption, OTP, IP-restricted login, audit trails. We follow all OWASP Principle to make our applications secure.
LIMS + MagicalQR + DMS + Audit Management + CRM. integrated platform handles all compliance needs for ISO 17025 , 15189 laboratories, 17011 organisations, healthcare, manufacturing, certification bodies, Inspection bodies and Government organizations.
Teams adopt it on day one. No steep learning curve. Familiar interface with powerful automation underneath. Drives immediate productivity gains.
We don’t just talk solutions—we deliver them. Here are proven examples of how we’ve transformed lab operations, eliminated audit gaps, and accelerated accreditation for labs just like yours.
Transformer Oil Testing Laboratory was relying heavily on manual reporting, spreadsheet-based calculations, and traditional documentation methods.
Complex mathematical computations, client-specific report formats, and manual approval processes made it difficult to maintain accuracy, consistency, and strict ISO/IEC 17025 compliance.
✓ Full ISO/IEC 17025 compliance achieved
✓ 70–80% reduction in report preparation time
✓ Zero manual calculation errors
✓ Improved client satisfaction with accurate, customizable reports
Deployed a custom-built ISO/IEC 17025-compliant CPD LIMS with automated report generation, dynamic report templates, role-based approval workflows, and centralized data management.
Integrated automated calculations, full audit trails, and secure access controls to ensure end-to-end traceability and accreditation alignment.
The automotive OEM manufacturing shock absorbers relied on manual tracking across assembly and suspension testing, leading to errors, delays, and limited production visibility. There was no automated sequence validation or digital linkage between assembly and test data, affecting quality control and traceability.
✓ Reduced production cycle time
✓ Improved first-pass quality
✓ 100% end-to-end traceability
✓ Faster fault identification
✓ Real-time operational visibility
CPD Technologies implemented a barcode-based QA and traceability system with automated assembly validation, real-time suspension test data capture, and centralized monitoring dashboards. Each unit was uniquely tracked from assembly to final testing.
The Mineral, Coal & Coke Testing Laboratory was managing high sample volumes through manual data entry, paper-based logs, and spreadsheet-driven calculations.
Instrument outputs and Excel data were not integrated, leading to repetitive work, calculation errors, and delayed report generation.
✓ 70% faster report turnaround
✓ 90% reduction in manual errors
✓ 3X increase in testing capacity
✓ Improved data accuracy and compliance
✓ Real-time visibility and instant data accessibility
Implemented a customized ISO/IEC 17025-compliant LIMS to digitize all laboratory operations.
The system integrated instrument and Excel-based data into a unified platform, bulk sample processing, enabled built-in calculation engines, and provided instant report generation. Centralized record management and complete audit trails ensured full traceability and regulatory alignment.
The laboratory was performing chemical analysis using a spectrometer that generated test results in XML files. However, laboratory staff had to manually review instrument outputs, verify limits, determine the applicable test scope and method, and prepare raw data sheets and final reports.
This manual workflow increased the chances of errors, consumed significant time, and created delays in report generation while ensuring compliance with defined test limits and validation requirements.
✓ Automated processing of spectrometer XML files
✓ Elimination of manual data entry and calculation errors
✓ Instant generation of raw data sheets and test reports
✓ Automatic validation against configured limits and test scope
✓ Faster reporting and improved laboratory efficiency
CPD LIMS was implemented with a configuration to process instrument output files directly. Users upload the spectrometer-generated XML file into the system, where LIMS automatically reads and extracts the instrument data.
The system maps the instrument values to predefined test parameters, validates them against configured limits, and automatically determines the applicable test scope and method. Based on this validation, LIMS generates structured raw data sheets and prepares the final test report without manual calculations.
Skip the research—talk to our compliance
experts who understand NABL accreditation, ISO/IEC 17025,
FDA, GLP, and quality management at scale.
CPD’s approach is built on three interconnected pillars that work together to ensure your lab achieves and maintains world-class accreditation. Every solution we build is anchored in these core principles.
Eliminate manual spreadsheets and data entry errors. Our solutions transforms how business process works with Excel-like simplicity and enterprise-grade power.
Your lab’s data is protected with ISO 27001:2022 certified infrastructure. Zero compromises on security. Zero data breaches. Zero peace-of-mind compromises.
Over 50 accredited labs trust CPD for accreditation success.
We don’t just meet standards—we exceed them with continuous compliance.
4-6 Weeks Implementation
Fastest to Value
For organisations wanting immediate results without IT infrastructure investment.
Perfect for quick accreditation wins.
8-10 Weeks Implementation
Best Flexibility
For organisations with specific security or compliance requirements.
Full control with cloud convenience.
Need a custom setup?
+91 88001 59719
and expert guides on NABL accreditation, ISO 17025 compliance, lab automation, and quality management systems. Learn how CPD Technologies transform compliance into competitive advantage.








"We are extremely satisfied with the LIMS implementation process. Following our order in January 2025 and an intensive nine-month trial period, the system went live in November 2025 and has been running smoothly for the first month without major issues. The support from your team was exceptional: technical issues were attended to quickly with highly effective solutions, demonstrating far better responsiveness than expected. We particularly appreciate the extraordinary support provided by your developers during the heavy and complex customization phase; they worked incredibly hard, and the final output is excellent. The Business Analyst/Coordinator, in particular, was fantastic—her performance, attention, understanding of our business, and friendly communication were truly excellent throughout. Thank you for this highly successful partnership."
"Regarding the ULR & QR Code Generator Tool, my experience so far has been quite good. The tool is user-friendly, and it makes the process much more convenient and time-saving. Overall, I’m satisfied with the tool and appreciate your team’s efforts in developing it."