Pharma­ceutical.

Cold chain, serialisation and expiry under control — with the audit trail regulators ask for, generated automatically.

Request a consultation
Challenges we address
  • Cold chain complianceTemperature control through storage and transport, to protect efficacy.
  • Drug serialisationTracing individual units to deter counterfeiting.
  • Regulatory complianceFDA, EMA and local requirements, with audit trails and documentation.
  • Expiry managementExpiry dates and FEFO rotation to reduce waste and protect patients.
The floor, in layers

How Inventrack runs a GMP site.

L1 + L3 · Serialised stock, cold room, door alert
  1. Serialisation, by RFID Unique tags follow each unit from manufacture to delivery, with GS1-compliant data. RFID hardware →
  2. Temperature and humidity, by sensor Continuous monitoring with instant deviation alerts. Cold chain monitoring →
  3. Expiry and FEFO Alerts for approaching expiry dates and routing that rotates stock correctly. Inventory management →
  4. Automated compliance reporting Audit trails and regulatory reports covering movements, excursions and handling. Inventrack 6.0 →

Make your next audit routine.