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Stability You Can
Trust, Compliance
You Can Prove

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VaultGXP is your all-in-one Digital Pharma Solution

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STABILITY PROGRAM

A stability program in a laboratory, particularly within the pharmaceutical or biotechnology industry, is a systematic approach to assess how a product's quality changes over time under different environmental conditions.

  • Designed for Compliance. Built for Confidence.
  • Structured Studies with Real-Time Oversight
  • Reliable Data. Confident Decisions

Designed for Compliance. Built for Confidence

VaultGxP’s Stability Program enables organizations to design, manage, and track stability studies in full alignment with global regulatory guidelines (ICH, FDA, WHO, etc.). Whether it's for drug products, raw materials, or packaging components, the module handles long-term, accelerated, and ongoing studies with structured workflows, automated alerts, and pre-configured templates. From study initiation to final reporting, every activity is documented and auditable—ensuring data integrity and regulatory readiness at every stage.

DMS software interface

Structured Studies with Real-Time Oversight

The platform offers complete visibility into stability protocols, sample pulls, testing schedules, and results. Users can define storage conditions, time points, batch details, and pull criteria with precision. Real-time dashboards and reports help QA, QC, and regulatory teams monitor progress and identify potential risks early. By centralizing data and standardizing processes, VaultGxP eliminates manual tracking and spreadsheets—reducing errors and improving traceability across global stability programs.

Reliable Data. Confident Decisions.

All stability data is securely captured, version-controlled, and linked with testing outcomes and batch records. With built-in audit trails, electronic signatures, and automated notifications, the Stability Program ensures every decision is backed by accurate, validated data. VaultGxP empowers quality-driven teams to make confident, timely decisions on product shelf-life, specifications, and release—ensuring products stay safe, effective, and compliant throughout their lifecycle.

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.