Pharmaceutical manufacturing demands total traceability, GMP compliance and audit readiness at every step. Teamnet embeds regulatory requirements into your workflows — not as an afterthought, but as the foundation.
GMP, WHO-GMP, FDA 21 CFR Part 11 — every batch needs electronic records, deviation tracking and audit trails. Manual systems cannot keep up.
Temperature excursions during storage or transit can destroy entire batches. Real-time monitoring is not optional — it is regulatory.
If a quality issue surfaces post-distribution, you need to trace every raw material, every process step and every shipment in minutes, not days.
From raw material receipt to finished goods release — every step documented, every deviation tracked, every batch traceable.
Batch production with stage-gate quality checks, in-process testing, deviation management and electronic batch records. GMP-ready workflows.
Chemical inventory with SDS management, environmental monitoring, spill reporting and regulatory compliance. Protect your people and your licence.
Cold chain warehouse management with temperature monitoring, quarantine zones, expiry tracking and first-expiry-first-out picking.
Real-time temperature, humidity and pressure monitoring across cleanrooms, storage areas and transit. Automated alerts on threshold breaches.
Track pharmaceutical waste, energy consumption and carbon emissions. Generate sustainability reports for regulatory and investor audiences.
Access control for restricted areas, visitor management for auditors and contractors, and complete audit trail of facility access.
Every pharmaceutical workflow, built for compliance.
Quality data flows into production. Environmental data flows into compliance. Batch data flows into distribution. One database, full traceability.