AmpleLogic eLogbook

Electronic Logbook Software

Digitize Your Operations with AmpleLogic e Logbook

AmpleLogic e Logbook revolutionizes data management in regulated industries such as Life Sciences, Food & Beverages, Cosmetics, Gene Therapy, Medical Devices, and more. Our web-based software replaces manual logbooks, guaranteeing compliance, efficiency, and transparency in your operations.

Compliance at its Core

Stay compliant with our FDA-approved eLogbook, meeting 21 CFR Part 11 and other global regulatory standards.

Streamlined Operations

Our e Logbook streamlines your production process by managing equipment usage and quality control, eliminating inefficiencies for optimal efficiency.

Real-time Visibility

Track schedules, due dates, and activities effortlessly with a calendar display for insightful operations management, ensuring nothing slips through the cracks.

Automated Notifications

Stay on top of critical tasks with automated notifications and escalations, guaranteeing timely authentication and assessment of logs.

eLogbook

Why choose AmpleLogic e Logbook?

In an era of evolving regulations and complex manufacturing processes, AmpleLogic e Logbook stands out as the solution of choice. Our state-of-the-art software ensures:

Efficiency

Streamline your operations, reduce manual efforts, and save time.

Compliance

Meet the highest regulatory standards with a solution crafted for FDA and global regulatory requirements.

Transparency

Gain real-time visibility into your processes, from production to quality control.

Automation

Experience a seamless, paperless environment that enhances accuracy and reliability.

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Streamline Data Management with AmpleLogic e Logbook

Unlock the full potential of AmpleLogic eLogbook with these key features

Compliance Assurance

Maintain regulatory compliance with our FDA-compliant solution, adhering to 21 CFR Part 11 and other industry standards.

Version Control

Implement version control for documents and procedures to track changes, revisions, and approvals systematically.

Training and Competency Records

Maintain records of employee training and competency assessments to ensure a skilled and compliant workforce.

Maximum traceability

End to End progress and activity progress can be tracked in the system.

Equipment Usage and Maintenance

Track equipment usage logs, maintenance schedules, and performance data to optimize equipment efficiency and regulatory compliance.

Area Monitoring and Control

Implement monitoring and control features for pharmaceutical manufacturing areas (cleanrooms, production zones) to ensure compliance with environmental conditions.

Cleaning and Alarms

Cleaning schedules can be triggered based upon its frequency. Alarms for batch can be triggered .

Roles and Departments

Role wise logbooks and Department wise logbooks can be configured and can maintain logbook system site wise.

Enhanced Analytics

Effective reports for all the roles to display meaningful patterns of data in respective areas.

Integrations

Easy integration with various other quality systems to fetch required information.

Automated Notifications

Receive timely alerts and escalations for critical tasks, ensuring nothing is overlooked.

QR & Barcode Scanning

Usage of QR codes and BAR codes to ensure Data accuracy and integrity.

Verification

Validate resources like equipment, room, solutions before usage to avoid noncompliance.

Document Management

Efficiently manage documents, SOPs and records, reducing the risk of errors and data loss.

Customizable Reports

Generate tailored reports for management and compliance purposes, providing valuable insights into your operations.

Real-time Monitoring

Monitor operations in real-time, enhancing transparency and decision-making.

Data Integrity

Ensure the integrity of your logbook data, eliminating risks associated with manual record-keeping.

Workflow Automation

Streamline approval workflows, enhancing the accuracy and efficiency of data entry and validation.

Create Audit Trails

Automatically generate detailed audit trails for all actions and data entries within the eLogbook system, ensuring traceability and accountability.

User-friendly Interface

Experience an intuitive interface that simplifies logbook management for users at all levels.

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The AmpleLogic eLogbook Software/Electronic Logbook guarantees that information is disseminated throughout the organization’s essential operational departments including the quality, production, planning, and maintenance departments; and they serve to bring clarity and transparency to the entire organization’s production and QC lab activities.

AmpleLogic’s Electronic Logbook Software helps in configuration of different types of logbooks.

Area and Equipment Logbook

Equipment Usage logbookBoiler Operation logbook
Environment ConditionHPLC Usage logbook
Calibration LogbookAHU Parameter Monitoring
Chiller Operation logbookHEPA Filter Replacement
Purified Water DistributionAir Compressor Monitoring
Semi-Micro Balance logTDS Analyzer logbook
Pressure MonitoringMelting Point Apparatus
Electrical Substation OperationMaintenance logbook

Quality Control Logbook

Sample Registration logbookStability Protocol logbook
Chemical initiation logbookChemical Booking logbook
Sample Management LogbookStandard log
Impurity Standard logWorking standard log
Reference Standard logLaboratory standard log
Column Usage logIncubation log
Experiment template logSample Withdrawal log
Pilot experiment logGC Usage log

Documentation Logbook

Document Issuance logbookQuality observation log logbook
Request Issuance, Retrieval logExtension request for OOC log
Training Material IssuanceBatch Detail log
Training attendance logbookPacking Material logbook

Cleaning and Sanitation Logbook

Weekly Drain Point sanitationAccessories cleaning Log logbook
In-Process Container CleaningSequential Log
Portable equipment logDaily cleaning or sanitation
Modules

Alarm Management Module

AmpleLogic eLogbook

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Frequently Asked Questions

Our eLogbook offers a comprehensive digital solution, replacing manual paperwork with automated processes, ensuring accuracy and compliance.

Yes, our eLogbook is fully compliant with FDA regulations, including 21 CFR Part 11, ensuring the highest standards in electronic record-keeping.

By automating tasks, providing real-time visibility, and streamlining workflows, eLogbook significantly reduces manual efforts and enhances overall efficiency.

Absolutely. Our eLogbook is designed with flexibility in mind, allowing for customization to meet the unique requirements of different industries and organizations.

Security is a top priority. eLogbook employs robust measures to ensure data security and integrity, preventing unauthorized access and maintaining the accuracy of logbook entries.

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Your Pharma Automation Starts Here

We’re here to address your inquiries and assist you in identifying the solutions that best align with your requirements. Here’s why choosing us is your strategic advantage:

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