Pharmaceutical WMS for Latin America
Lot-level traceability, cold chain, FEFO/FIFO, and quarantine workflows — aligned with ANVISA (Brazil), INVIMA (Colombia), DIGEMID (Peru), ARCSA (Ecuador), and FDA.
Regulatory authorities covered
- ANVISA (Brazil) — RDC 430/2020, SNGPC for controlled substances
- INVIMA (Colombia) — Good Distribution Practices (GDP) and lot traceability
- DIGEMID (Peru) — pharmaceutical product registry and traceability
- ARCSA (Ecuador) — sanitary registration and controlled substances
- FDA (USA / Puerto Rico) — DSCSA serialization and cold chain
- DGI / Ministerio de Salud (Panama) — pharma distribution compliance
Technical capabilities for pharma
- Lot tracking to individual unit with complete traceability
- Temperature zones (ambient, 2–8°C, -18°C, -70°C) with IoT sensor integration
- FEFO (First Expiry First Out) as the default picking rule
- Quarantine → QA review → release workflow
- Controlled substances in vaulted locations with dual-authorization picking
- Recall workflow identifying every unit of an affected lot in minutes
- Regulatory audit reports exportable per authority
Who it serves
- Pharmaceutical distributors and wholesalers
- Hospital pharmacy networks
- Pharmacy chains with centralized distribution
- CRO/CMO pharmaceutical logistics
- Vaccine and biological cold-chain operations