Electronic Logbook Software (eLogs) for Pharmaceutical, CRO & Life Sciences

Replace Paper Logbooks with Secure, Compliant and Fully Digital Electronic Logbooks

Neopharmtech eLogs is a modern Electronic Logbook solution designed specifically for pharmaceutical companies, CROs, bioanalytical laboratories, manufacturing facilities, quality control laboratories and other regulated life science organizations.

It replaces paper-based equipment logbooks, instrument usage logs, cleaning records, maintenance logs, calibration records, environmental monitoring logs, and laboratory registers with a secure electronic platform.

Designed to support 21 CFR Part 11, EU Annex 11, ALCOA+, GxP, and global regulatory requirements, eLogs helps organizations improve compliance, eliminate manual documentation, and maintain complete traceability across all operational activities.

Challenges in Quality Management

Our Solution – Electronic Logs (eLogs)

Neopharmtech eLogs digitizes all laboratory and manufacturing logbooks into a centralized electronic platform.

  • Equipment Usage Logs
  • Instrument Logbooks
  • Calibration Logs
  • Maintenance Logs
  • Cleaning Logs
  • Breakdown Logs
  • Temperature Monitoring Logs
  • Environmental Monitoring Logs
  • Utility Logs
  • Area Cleaning Records
  • Daily Laboratory Registers
  • Shift Handover Logs
  • Asset Movement Logs
  • Preventive Maintenance Logs
  • Validation Activity Logs

using configurable workflows, electronic signatures, audit trails, automated notifications and role-based approvals.

Our solution improves compliance, enhances productivity and ensures every activity is documented accurately.

Key Features & Benefits

Equipment Usage Logbook

Feature: Record equipment usage electronically with operator details, project, batch number, date, time and remarks.

Benefit: Provides complete utilization history of every equipment.

Business Impact: Improves equipment traceability and inspection readiness.

Cleaning Logbooks

Feature: Digitally record equipment and area cleaning activities.

Benefit: Ensures standardized cleaning documentation.

Business Impact: Reduces documentation errors and supports GMP compliance.

Calibration & Maintenance Logs

Feature: Track calibration schedules, preventive maintenance and breakdown history.

Benefit: Automated reminders prevent overdue activities.

Business Impact: Improves equipment uptime and regulatory compliance.

Electronic Signatures

Feature: Secure electronic signatures with reviewer approvals.

Benefit: Eliminates manual signatures and paper approvals.

Business Impact: Supports 21 CFR Part 11 compliance.

Audit Trails

Feature: Automatically records every modification with user, date, time and reason.

Benefit: Provides complete transparency.

Business Impact: Simplifies regulatory inspections.

Workflow Automation

Feature: Configurable approval workflows with automated notifications.

Benefit: Accelerates review and approval.

Business Impact: Improves operational efficiency.

Role-Based Access Control

Feature: User-specific permissions and controlled access.

Benefit: Ensures only authorized personnel can perform activities.

Business Impact: Improves security and data integrity.

Why Choose Neopharmtech eLogs?

Eliminate Paper Logbooks

Digitize quality workflows and eliminate paperwork through automated approvals and configurable workflows.

  • Go completely paperless
  • Reduce documentation errors
  • Faster reviews
  • Centralized records

Improve Regulatory Compliance

Designed specifically for regulated pharmaceutical and life science organizations.

  • 21 CFR Part 11
  • EU Annex 11
  • ALCOA+
  • GxP
  • Audit Trails
  • Electronic Signatures

Improve Operational Efficiency

Detect quality issues early, implement CAPA effectively and drive continuous improvement.

  • Automated workflows
  • Notifications
  • Equipment tracking
  • Digital approvals

Enterprise Ready

Scalable architecture suitable for growing pharmaceutical organizations.

  • Multi-site support
  • Multi-department support
  • Cloud or On-Premise deployment
  • Configurable workflows
  • Integration with existing systems

Industries We Serve

  • Pharmaceutical Companies
  • CROs
  • Bioanalytical Laboratories
  • Biotechnology Companies
  • Medical Device Manufacturers
  • Contract Manufacturing Organizations
  • Research Laboratories
  • Quality Control Laboratories
  • API Manufacturers
  • Manufacturing Facilities

Frequently Asked Questions

What is an Electronic Logbook?

An Electronic Logbook (eLogs) is a digital system used to replace paper logbooks for recording equipment usage, maintenance, cleaning, calibration and laboratory activities while ensuring complete traceability.

Is eLogs compliant with 21 CFR Part 11?

Yes. Neopharmtech eLogs supports electronic signatures, audit trails, secure authentication and role-based access to help organizations comply with 21 CFR Part 11 and other regulatory requirements.

Which logbooks can be digitized?

eLogs can digitize equipment logbooks, calibration logs, maintenance logs, cleaning logs, environmental monitoring records, utility logs, laboratory registers, temperature logs and many other operational records.

Is eLogs suitable for multi-site organizations?

Yes. The platform supports multiple sites, departments and facilities from a centralized environment.

Get Started

Ready to Replace Paper Logbooks?

Transform manual logbooks into secure, compliant electronic records with Neopharmtech eLogs.

Schedule a free product demonstration today and discover how eLogs improves compliance, enhances operational efficiency and simplifies regulatory inspections.

Neopharmtech India Private Limited

#109, Bhavya Majestic Enclave,
Madhava Nagar Colony,
Miyapur, Hyderabad, Telangana 500049