Pharmaceuticals & Life Sciences

Compliance Meets
Digital Efficiency.

Digitize your logbooks and environment monitoring. Ensure 21 CFR Part 11 compliance, data integrity, and audit readiness without the paper trail.

Errors Reduced 100%

Challenges in Pharma Manufacturing

Data Integrity Gaps

Manual paper logs are prone to errors, illegible handwriting, and are difficult to defend during FDA audits.

Environment Deviations

A spike in humidity or temperature can ruin an entire batch if not detected immediately.

Batch Traceability

Retrieving historical data for a specific batch number takes hours of digging through file cabinets.

The Forlyze Solution

Secure, encrypted, and automated data capture for regulated industries.

Digital Logbooks (e-Log)

Tablet-based entry for operators. Auto-captures machine data with unalterable timestamps.

Wireless Environment IoT

Real-time sensors for Temp/RH/Differential Pressure. Instant WhatsApp alerts on deviation.

Audit-Ready Reports

Generate PDF reports for any date range or batch number in seconds. 21 CFR Part 11 compliant.

> System Check: 21 CFR Compliance... OK
> Room: Blister Packaging Area
Temperature
22.4 °C
Humidity
45% RH
Last calibration: 12 Oct 2024