AmpleLogic eLogbook

Electronic Logbook Software

Digitize Your Operations with AmpleLogic e Logbook

Digitize Logbook Journey in Lifesciences

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.

Document Management

Efficiently manage documents, SOPs, and records to reduce errors and data loss

Equipment Usage and Maintenance

Track equipment usage, maintenance schedules, and performance data with AmpleLogic electronic log book

Area Monitoring and Control

Implement monitoring and control for cleanrooms and production zones

Training and Competency Records

Maintain employee training and competency records

Why choose AmpleLogic Electronic LogBook?

In an era of evolving regulations and complex manufacturing processes, AmpleLogic eLogbook stands out as the solution of choice. Our state-of-the-art software ensures essential data is disseminated throughout the organization’s essential operational departments to bring clarity and transparency to the entire organization’s production.

Streamlined Operations

Optimize production process by managing equipment usage and area control

Real-time Visibility

Track schedules, due dates, and activities effortlessly with a calendar display

Automated Notifications

Automated escalations guaranteeing timely authentication and assessment of logs

Compliance at its Core

Stay compliant with USFDA 21 CFR Part 11 and other global regulatory standards

Shape dots arrow right

Streamline Data Management with AmpleLogic e Logbook

Unlock full potential of AmpleLogic Electronic logbook (eLogbook) with these key features

Competency Records

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

Equipment Data

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

Area Data

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

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

Version Control

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

Enhanced Analytics

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

System Integration

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 non-compliance

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

Facilitates Verification

Validate resources like equipment, room, solutions before usage to avoid non-compliance

Smart Reports

Complex data will be displayed in simple custom reports for easy understanding of data

Interactive Dashboard

Infographic Dashboard for crucial insights like resource occupancy, performance etc

Interlocking

Equipment Interlocking, Operator Interlocking, Due dates interlocking can be configured

Access from Any Device

Accessible from multiple devices like mobile phone, tablet, laptop

User Tracking

User scheduling and activity tracking performed by the user

Offline Access

Application can be accessed in offline mode as well

Compliance Assurance

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

Shape dots arrow right

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 the 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

Articles

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.

Contact us

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:

Your benefits:
What happens next?
1

Schedule a call at your convenience 

2

Discovery and consultation session

3

Get your custom proposal

Schedule a Free Demo
Request a Demo