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From Creation
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VaultGXP is your all-in-one Digital Pharma Solution

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DMS

DOCUMENT MANAGEMENT SYSTEM

software that manages the storage, organization, and retrieval of digital documents and records. It essentially acts as a digital filing cabinet, allowing businesses to streamline document-related processes, improve accessibility, and enhance security.

  • Controlled Documents-Compliant Processes
  • Streamlined Collaboration-Secured Access
  • Be Inspection-Ready-Always

Controlled Documents-Compliant Processes

VaultGxP’s Document Management System (DMS) offers a centralized, GxP-compliant platform to manage SOPs, protocols, work instructions, and quality documents with full control and traceability. Built to meet regulatory standards like 21 CFR Part 11 and EU Annex 11, it ensures version control, electronic signatures, and controlled access across your organization.

DMS software interface

Streamlined Collaboration-Secured Access

The DMS supports collaborative editing, parallel reviews, and configurable approval hierarchies—eliminating bottlenecks and maintaining document integrity. Role-based access controls ensure that only authorized personnel can access or edit content, with real-time tracking of document status, reviewer comments, and change history.

Be Inspection-Ready-Always

VaultGxP’s DMS ensures audit readiness with complete document trails, version history, and secure archiving. Integrated dashboards provide visibility into pending reviews, overdue tasks, and controlled document distribution. The system also links documents to quality events such as deviations, CAPAs, or training records.

Quick Guide to Our Solutions
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Stability Program

The VaultGxP Stability Program within a digital system provides a comprehensive, streamlined solution for managing stability testing.

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Warehouse Management

Warehouse Management Systems (WMS) optimize storage, tracking, and operations across multiple locations.

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QMS & Risk Management

GMPs provide a detailed roadmap for maintaining quality in drug production. These crucial guidelines dictate how manufacturers.

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Electronic Lab Notebook

Electronic Lab Notebook software digitizes laboratory workflows, enabling researchers to securely record, organize, share data.

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Deviation Management

Deviation Management is an essential process within Quality Management Systems (QMS), particularly in regulated industries.

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Laboratory Incident

In laboratory environments, particularly in regulated industries such as pharmaceuticals, biotechnology.

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Computer System Validation

VaultGxP's Computer System Validation ensures compliance with critical regulatory standards such as FDA 21 CFR Part 11 and GXP.

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Calibration & PM Program

The VaultGxP Calibration and Preventive Maintenance (PM) Program offers a digital solution that enhances the management.

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Regulatory Compliance

VaultGxP streamlines regulatory compliant, ensuring efficient, compliant submissions to global bodies like FDA, EMA, and PMDA.

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Change Management

Change Management is a critical process for any organization, particularly in dynamic industries like life sciences.

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Smart Audit

Smart Audit is a critical component of maintaining quality and compliance within regulated industries like pharmaceuticals.

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Learning Management

Empower Your Training with E-Learn" is a powerful tagline or slogan for promoting an e-learning platform or solution.

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OOS/OOT and Reporting

In industries like pharmaceuticals, biotechnology, and other regulated sectors, ensuring that products meet quality.

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Sample Management System

Sample Management covers the entire lab sample lifecycle—from login to generate a certification.

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QC Laboratory Services

Laboratory layout design services focus on optimizing space utilization, workflow efficiency, and safety by integrating.