Pharma QMS
Trusted by Leading Pharmaceutical Companies

Complete Quality Management System for Pharma & Life Sciences

Streamline compliance, quality control, and documentation with our integrated QMS, DMS, and LIMS solutions. Built for USFDA, EMA, MHRA, and 21 CFR Part 11 compliance.

Quality Management System

Pharma QMS - Quality Management System

Centralized quality management platform enhancing compliance and risk control across the product lifecycle

Change Control
Manages evaluation, approval, and implementation of controlled changes.
CAPA (Corrective and Preventive Action)
Identifies the root cause of an issue and implements corrective actions to fix it and preventive actions to avoid recurrence.
Audit Management
Plans, executes, and tracks internal/external audits and findings.
Supplier Quality
Qualifies, monitors, and audits suppliers and materials.
Equipment/Calibration
Manages equipment lifecycle, calibration, and maintenance compliance.
Batch Record Management
Maintains electronic batch manufacturing/packaging records with review.
Document Management

DMS - Document Management System

Centralized system for controlling, approving, and maintaining all GMP documents

Document Creation & Authoring
Creates new controlled documents like SOPs, policies, and work instructions.
Document Review & Approval Workflow
Routes documents through reviewer and approver stages before release.
Version Control & Updates
Maintains document revisions, history, and ensures only the latest version is active.
Document Issuance / Distribution
Releases approved documents to departments in a controlled manner.
Document Templates Management
Maintains reusable templates for SOPs, reports, forms, etc.
Audit Trail / History Log
Maintains reusable templates for SOPs, reports, forms, etc.
Laboratory Management

LIMS - Laboratory Information Management System

Supports sample tracking, test execution, instrument management, data integrity, and reporting

Sample Management
Tracks samples from registration to disposal, ensuring full traceability across all lab activities.
Instrument Management
Manages laboratory instruments, including calibration, maintenance, and usage logs for compliance
eLog

Electronic Logbook

Digital, automated logbooks for equipment and process tracking across all operations

Comprehensive Tracking
  • Production equipment logs
  • QA/QC process tracking
  • Warehouse operations
  • Environmental monitoring
Smart Features
  • Customizable log formats
  • E-checklists for operations
  • Windows and Android tablet support
  • Seamless data exchange
Regulatory Compliance

Built for Compliance

Our solutions meet the highest industry standards and regulatory requirements

USFDA
FDA Compliant
EMA
European Standards
MHRA
UK Regulation
21 CFR Part 11
E-Signature Compliant

Ready to Transform Your Quality Management?

Join leading pharmaceutical companies using Pharma QMS to streamline compliance and boost efficiency