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Cold chain integrity from production to patient.

GDP-compliant temperature monitoring for pharmaceutical manufacturing, distribution, and last-mile delivery — built around the regulatory environments that govern your supply chain.

Temperature excursions cost the industry billions every year.

  • WHO estimates 25% of vaccines arrive degraded due to cold chain failures.
  • Pharma temperature deviations trigger product holds and recall costs averaging $10M+ per incident.
  • Manual log spreadsheets fail FDA 21 CFR Part 11 audits.

Continuous, audit-ready visibility — without adding headcount.

  • Real-time alerts before product reaches the threshold of damage.
  • Tamper-proof records that satisfy FDA, EMA, MHRA, and PMDA inspectors.
  • Integration with your existing ERP, WMS, and quality systems.
01 · HARDWARE

Dataloggers and gateways engineered for pharmaceutical environments — −200°C to +150°C, validated to your protocols.

02 · ZTMS CLOUD

Real-time dashboards, automated GDP/Part 11 reports, REST API into your QMS, ERP, and WMS.

03 · REGIONAL SUPPORT

Dedicated specialists in San Francisco and Düsseldorf. Validation support, deployment, and audit assistance.

Each ZKSCool deployment includes IQ/OQ/PQ validation documentation, calibration certificates traceable to NIST/PTB standards, and audit trail exports compliant with FDA 21 CFR Part 11 and EU GDP §6.