Industrial Data Logger For Pharma Compliance

Automate your GMP, GDP, and 21 CFR Part 11 monitoring with our high-precision logging systems designed for the most stringent pharmaceutical environments.

Get Quote Technical Specs
Used by pharma manufacturers
Designed for audits & regulatory inspections
Built in India for global compliance

What Is a Data Logger for Pharma?

A Data Logger for the pharmaceutical industry is an electronic system designed to record and store critical parameters such as temperature, humidity, pressure, and equipment status in a secure, traceable, and audit-ready format.

Tamper-Proof

Secure, encrypted data that cannot be modified.

Time-Stamped

Every log is recorded with precise server time.

Secure Access

Role-based logins ensuring data integrity.

Audit Trails

Full history of system interactions and logs.

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Pharma Data Logger Device
24/7 Continuous Monitoring
Data Logger for Pharma
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Data Logger for Pharma

Starts from ₹25,000 ₹27,999
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Data Logger for Pharma by AIOTHUB records multiple parameters simultaneously, reducing hardware costs while delivering synchronized data, centralized monitoring, scalable expansion, precise analysis, faster decisions, and improved operational efficiency.

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SKU: AIOT-DL-MC-2025
Category: Industrial Hardware
Tags: IoT, Pharma, Automation
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1 Year Warranty
24/7 Support

Compliance & Operational Features

Our Data Logger for Pharma is engineered specifically to meet the high standards of the pharmaceutical industry, providing a reliable foundation for all your monitoring and compliance needs.

Feature Benefit
21 CFR Part 11 Compliance Audit-ready electronic records with full traceability.
Encrypted Data Storage Prevents unauthorized access and data manipulation.
Real-Time Monitoring Early detection of deviations to ensure safety.
Automated Alerts Proactive protection for critical batches and vaccine storage.
Calibration Support Guarantees continuous regulatory and standard compliance.
Automatic Data Backup Ensures zero data loss during power or network outages.
User Access Control Maintains absolute data integrity through role-based security.
Enclosure IP65 Industrial (Cleanroom safe)
Mounting Wall / DIN Rail
Connectivity 4G LTE Cat-M, Wi-Fi, Ethernet
Input Voltage 9–36 VDC with 72+ Hour Battery Backup
Operating Temp −40°C to +85°C
Security AES-256 Encryption, TLS 1.3, Secure Boot

Pharma-Grade Technical Specifications

Pharmaceutical manufacturers must comply with stringent regulations, including FDA 21 CFR Part 11, Good Manufacturing Practices (GMP), and ISO 13485. Our system is engineered to exceed these requirements.

Parameter Specification Why It Matters in Pharma
Core System
Microcontroller 32-bit Industrial MCU Stable long-term operation
RTC Accuracy ±2 ppm with battery backup Valid timestamps for audits
Time Sync NTP CFR-compliant time integrity
Watchdog & Brownout Enabled No missing data
Temperature Measurement
Sensor Type PT100 / PT1000 / Thermocouple Regulatory-approved sensors
Accuracy ±0.1°C (PT100) Vaccine & drug safety
Resolution 0.01°C High precision
Calibration 2-point or 3-point calibration Audit compliance
Humidity Measurement
Sensor Type Digital RH or Industrial Probe Stability testing
Accuracy ±1.5 %RH Stability & cleanroom
Compensation Temperature compensated Reliable readings
Analog Inputs
Resolution 24-bit ADC Lab-grade precision
Input Types 0–10V, 4–20 mA Pharma equipment compatibility
Isolation Galvanic isolation Prevents electrical noise
Digital Interfaces
RS-485 Modbus RTU Freezers, BMS, PLCs
Ethernet Yes Validation-ready networking
Data Integrity
Storage 8–32 GB Industrial SD Card Years of logs
Backup Internal Flash Zero data loss
Data Format Encrypted CSV + JSON Audit & cloud ready
Checksums CRC + SHA256 Tamper detection
Regulatory Compliance
Audit Trail Every change logged 21 CFR Part 11
User Roles Admin / Operator / Auditor GMP control
Electronic Signature Yes Regulatory approval
Time-stamped Logs Non-editable Legal traceability
Alarms & Alerts
Limits High / Low / Deviation Cold-chain safety
Alerts Email, SMS, Cloud Immediate action
Local Alarm Buzzer & LED On-site warning
Validation Ready
IQ/OQ/PQ Support Available Regulatory validation
Calibration Certificate NIST traceable Audits
Data Export PDF, CSV Regulatory reports
Is this data logger 21 CFR Part 11 compliant?
Yes. It supports secure logins, audit trails, and tamper-proof electronic records.
Can it be used for vaccine storage and cold rooms?
Yes. It is widely used for vaccine freezers, cold rooms, and refrigerated transport environments.
Does it replace manual temperature logs?
Yes. It provides automatic, continuous digital records that are audit-ready.
How long is data stored?
Data can be stored for years, depending on your compliance and validation needs.
Can reports be used during audits?
Yes. Reports are formatted for GMP, GDP, and regulatory inspections.
Critical Compliance

Why Pharma Companies
Need an Industrial Data Logger

Manual temperature sheets, delayed data collection, and unverified records are no longer acceptable under GMP, GDP, and 21 CFR Part 11. Our system captures, secures, and reports your data automatically.

Our Data Logger Safeguards You From:

Failed Audits
Batch Rejections
Cold-Chain Risks
Regulatory Penalties

Designed for Global Pharma Compliance

Our system is built to meet the strict data integrity and traceability requirements of regulated pharmaceutical environments.

GMP

Continuous, validated data logging to ensure Good Manufacturing Practices.

21 CFR Part 11

Secure, electronic records with full audit trails for FDA compliance.

GDP

Meeting Good Distribution Practices for cold-chain and storage safety.

WHO

Adhering to World Health Organization standards for data traceability.

CDSCO

Audit-ready documentation compliant with Indian regulatory standards.
Hardware Specs

What Parameters
Can You Monitor?

Our system supports a wide range of industrial sensors, providing sub-degree accuracy for sensitive pharmaceutical environments.

Temperature

Range: -200°C to +400°C

Humidity

Range: 0% to 100% RH

Pressure

Differential Pressure

Power

Failure Alerts

Facility Security

Door Monitoring

Custom Config

Specialized Probes

Facility Integration

Where It Is Used in Pharma Facilities

Our data logging solutions are engineered for high-stakes pharmaceutical environments, ensuring total compliance and safety across every critical zone.

How the System Works?

A seamless flow from environmental monitoring to audit-ready compliance reporting.

1. Collection

Real-time monitoring of critical pharma parameters.

2. Transmission

Secure encryption and wireless data transfer.

3. Storage

Audit-ready, tamper-proof cloud storage.

4. Reporting

Automated GMP-compliant report generation.

5. Alerts

Instant multi-channel alerts for deviations.

Value Proposition

Why Pharma Companies Trust AIOTHUB

Generic temperature loggers often fall short of regulatory expectations. Our system is precision-engineered to meet the zero-tolerance requirements of pharmaceutical manufacturing and storage.

Audit-Ready Records

Generate secure, time-stamped reports that are instantly ready for FDA, GMP, and GDP inspections without manual intervention.

Validated Architecture

Built on a foundation of data integrity (ALCOA+ principles), ensuring your records are accurate, legible, and contemporaneous.

Risk Mitigation

Detect deviations in real-time. Prevent batch rejections and ensure the safety of vaccines and sensitive drugs through active monitoring.

Enterprise Scalability

From a single stability chamber to an entire multi-site manufacturing facility, our system scales with your operational needs.

Regulatory Confidence

Trusted by biotech leaders and cold-chain operators who require certified industrial-grade hardware and software solutions.

Automated Backups

Dual-redundant storage ensures zero data loss during power outages or network failures, maintaining a continuous audit trail.

Industrial Standard

This is not a consumer-grade device. It is a certified, regulatory-compliant monitoring system specifically architected for the high-stakes pharmaceutical and life sciences industries.

Compliance FDA 21 CFR

Make Your Pharma Facility Audit-Ready

Stop risking compliance with manual logs and incomplete records.
Move to a validated, automated, and secure Pharma Data Logger.

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