Our plc touch screen control pharmaceutical boiler system delivers precise steam generation for clean‑room sterilization, formulation heating, and GMP‑compliant batch processes. Engineered for continuous operation in regulated environments, the solution integrates a rugged PLC controller with an intuitive HMI, enabling real‑time monitoring, alarm management, and remote diagnostics—all within a single, compact footprint.
Designed for pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and equipment distributors, the system meets the strict validation and documentation requirements of the industry while offering flexibility for custom load profiles.
Typical specifications are provided below; all parameters can be customised to match your process requirements.
| Parameter | Range / Option | Unit |
|---|---|---|
| Steam Output | 50 – 500 | kg/h |
| Operating Pressure | 0.5 – 3.0 | MPa |
| Temperature Accuracy | ±0.2 | °C |
| Control Panel Size | 10” – 21” | inch (diagonal) |
| PLC Type | Modular IEC 61131‑3 | — |
| Material of Boiler Vessel | 316L Stainless Steel | — |
| Power Supply | 380‑415 V, 3‑phase | — |
| Warranty | 24 months | — |
The flexibility of the plc touch screen control pharmaceutical boiler system makes it suitable for a wide range of process steps where sterile steam or heated water is required.
We typically work with an MOQ of one complete unit, allowing you to order a fully customised solution that matches your specific steam capacity and control requirements.
Yes. The modular IEC 61131‑3 controller supports optional expansion racks, Ethernet/IP, and OPC-UA gateways for seamless integration with SCADA or MES platforms.
Standard configurations are shipped within 15‑30 days. Fully bespoke projects, including special material certifications, may require 30‑45 days depending on the scope.
A complete validation package—Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) reports—is supplied with every system, aligned with FDA 21 CFR 211 and EMA guidelines.
Ready to streamline your steam generation with a compliant, high‑performance solution?
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