Verifarma QMS

Verifarma QMS
Product Description

The platform enables the integrated management of deviations, CAPAs, change controls, audits, documentation, training, and risk management, providing full traceability, version control, and audit-ready records. Verifarma QMS replaces manual and fragmented processes with a unified, validated environment aligned with regulatory best practices.

Designed to scale alongside organizational growth, Verifarma QMS adapts to companies of different sizes and regulatory frameworks, helping quality teams reduce errors, improve operational efficiency, and ensure patient safety.

Verifarma International

  • Country/Region:
    Spain
  • On CPHI since:
    2026
Specifications
  • CAS Registry Number
    500
  • Details
    Verifarma QMS is Verifarma’s Quality Management System, specifically designed for the pharmaceutical, veterinary, and life sciences industries. The solution centralizes, digitizes, and controls all key quality processes, ensuring compliance with local and international regulations while promoting continuous improvement.

  • Selling Points
    Quality Service; Verifarma QMS provides a unified and validated platform to manage all quality processes in highly regulated environments. From deviations and CAPAs to audits, documentation, and training, the system ensures full traceability, compliance, and operational efficiency across the organization.

    Built to meet global regulatory standards such as FDA 21 CFR Part 11 and EU Annex 11, Verifarma QMS enables electronic signatures, audit trails, and secure data management, ensuring audit readiness at all times.

    With configurable workflows, real-time dashboards, and seamless integration with other systems, Verifarma QMS helps life sciences companies streamline operations, reduce manual errors, and scale their quality processes with confidence.

  • Model
    QMS
  • Supplied from
    Spain
  • Measured In
    US$

Verifarma International

  • Country/Region:
    Spain
  • On CPHI since:
    2026

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