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Keeping Your
Equipment Audit-
Ready, Always

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VaultGXP is your all-in-one Digital Pharma Solution

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CALIBRATION & PM PROGRAM

Instrument & Equipment Calibration Program

An instrument and equipment calibration program is a system designed to ensure the accuracy and reliability of measuring instruments and equipment used in various processes, particularly in industries where precise measurements are critical.

  • Precision Starts with Well-Calibrated Instruments-Plan with Clarity-Execute with Control.
  • Streamlined Scheduling with Full Lifecycle Control
  • Audit-Ready Records - Zero Compromise on Compliance

Precision Starts with Well-Calibrated Instruments.

VaultGxP’s Instrument & Equipment Calibration Program ensures that all laboratory and manufacturing equipment operate within defined accuracy and performance standards. It supports scheduling, execution, and documentation of calibration activities for a wide range of instruments—from analytical tools to critical production equipment. The system is fully GxP-compliant, offering built-in reminders, automated workflows, and escalation alerts to prevent missed calibrations. This ensures minimized downtime, improved reliability, and consistent quality in every operation.

DMS software interface

Streamlined Scheduling with Full Lifecycle Control

The module simplifies calibration planning by allowing users to define frequency, calibration methods, responsible personnel, and required documentation. Real-time dashboards offer insights into upcoming calibrations, overdue tasks, and calibration history, helping teams manage equipment proactively. Whether you're managing internal labs or third-party service providers, the program ensures traceability and structured compliance, reducing the risk of errors and non-conformance during audits or inspections.

Audit-Ready Records Zero Compromise on Compliance.

Each calibration event is securely recorded with time-stamped logs, technician details, reference standards, and electronic certificates. The system supports version control, role-based access, and tamper-proof data storage-ensuring your calibration records are always inspection-ready. VaultGxP’s Calibration Program reinforces your quality systems by delivering transparency, accountability, and regulatory alignment. It’s a powerful solution for organizations committed to operational excellence and equipment integrity in regulated environments.

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.