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Accuracy
in Every
Digital Entry

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VaultGXP is your all-in-one Digital Pharma Solution

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ELECTRONIC LOGBOOKS

Electronic logbooks (e-logbooks) are digital systems that replace traditional paper-based logbooks, offering a more efficient and secure way to record, manage, and analyze data in various industries. These systems are particularly beneficial in manufacturing, pharmaceuticals, and regulated industries where data integrity and traceability are crucial.

  • Digital-First Approach to Daily Operations
  • Consistent Records-Compliant Processes
  • From Routine Logs to Quality Insights.

Digital-First Approach to Daily Operations

VaultGxP’s E-Logbooks offer a modern, compliant alternative to traditional paper logbooks used in laboratories, manufacturing, and quality control environments. Whether for equipment usage, cleaning records, environmental monitoring, or shift handovers, the platform captures routine entries in a structured, secure, and time-stamped manner. It eliminates manual errors, enhances operational visibility, and ensures that logs are consistent, reviewable, and audit-ready—supporting day-to-day activities with greater accuracy and control.

DMS software interface

Consistent Records. Compliant Processes

Every log entry in VaultGxP’s E-Logbook is governed by defined templates, workflows, and access controls. Role-based authentication, electronic signatures, and built-in review mechanisms ensure only authorized users can make or verify entries. With automatic reminders for due tasks and alerts for missed entries, teams stay aligned with SOPs and regulatory expectations. This structured approach supports GxP, ALCOA+, and data integrity guidelines—making compliance a seamless part of routine operations.

From Routine Logs to Quality Insights.

The E-Logbook is more than just a digital replacement—it's a strategic tool that transforms operational data into actionable insights. With searchable records, trend analysis, and integration potential with other VaultGxP modules, teams can detect deviations, identify inefficiencies, and support continuous improvement. By digitizing and centralizing logs, organizations gain better traceability, reduce documentation burden, and improve audit preparedness—laying the foundation for smarter, quality-driven operations.

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.