ISO 17025 & ISO 15189 Laboratory Document Management System in India

Secure, clause-mapped, audit-ready Document Management System for laboratories, inspection bodies and ISO certified organizations.

100% Compliance

ISO 17025 & ISO 15189

Comprehensive ISO DMS for Laboratories

Say goodbye to paper-based chaos. Our DMS provides a single source of truth for all your standard operating procedures,
policies, and records, ensuring regulatory compliance is built into your everyday operations.

What is CPD DMS?

CPD DMS is a robust ISO 17025 Document Management System and ISO 15189 Laboratory Document Control Software designed to streamline quality documentation, ensure compliance with accreditation requirements and strengthen internal quality management systems.

Supported Standards

Our ISO compliant Document Management System supports ISO 9001, ISO 27001, ISO 17020, ISO 17021, ISO 22000 and other regulatory frameworks. Laboratories and certification bodies require structured document control, automated version tracking, approval workflows and secure role-based access to maintain compliance.

Why CPD DMS?

With CPD DMS, organizations eliminate manual documentation errors, reduce audit observations and maintain real-time traceability of SOPs, test methods, calibration procedures, management review records and corrective action reports.

Why ISO 17025 & ISO 15189 Laboratories Must Implement Digital DMS

Manual documentation puts your accreditation at risk. CPD DMS delivers structured, secure and fully traceable document control across all major ISO frameworks.

ISO 17025 Compliance

Maintain strict document control under Clause 7 and eliminate risks of outdated procedures, duplicate forms and audit non-conformities.

ISO 15189 Medical Labs

Ensure secure documentation, patient data protection and technical competence with full traceability and structured review mechanisms.

ISO 9001 & ISO 27001

Streamline document approval workflows and ensure encrypted, role-based secure access for sensitive organizational records.

Detailed benefits of CPD DMS

Everything your laboratory needs for structured, secure and audit-ready document control.

Automated version control

Full revision history with automated tracking of every document change.

ISO clause mapping

Map documents directly to ISO clauses for faster audit traceability.

Role-based access

Control who views, edits or approves documents with granular user permissions.

Secure cloud storage

Encrypted cloud-based repository for all your critical lab documents.

Public document links

Publish documents publicly with live embeddable links for easy sharing.

Comprehensive audit trail

Detailed logs of every document action for full accountability.

Review reminders

Automated alerts to notify teams when documents are due for review.

Compliance visibility

Real-time dashboard to monitor compliance status and accountability across teams.

Manual vs. Digital DMS

Comprehensive coverage ensuring nothing is missed from sample to report.

Feature Analysis Manual System Digital DMS
Data Accessibility Time-consuming physical searches
Instant retrieval with advanced search
Version Risk High risk of using obsolete versions
Automated control; only latest is active
Storage Requirements Extensive physical space & filing
Zero-footprint cloud/digital storage
Audit Preparation Weeks of manual gathering
Ready in minutes with reports

Frequently Asked Questions

Everything your laboratory needs for structured, secure and audit-ready document control.

Is CPD DMS suitable for NABL accredited laboratories?

Yes, it supports ISO 17025 and 15189 and other ISO clause mapping and audit readiness.

Yes, it follows ISO 27001 aligned security controls.

Yes, it supports structured medical laboratory documentation.