Custom Engineered Panel for Pharmaceuticals
IEC 61439 custom engineered panel assemblies engineered for pharmaceuticals applications. GMP-compliant IEC 61439 panel assemblies for pharmaceutical manufacturing, cleanrooms, and biotech facilities meeting validation requirements.
Custom Engineered Panel assemblies for pharmaceuticals combine IEC 61439 low-voltage switchgear design with hygienic construction, validation-ready documentation, and industry-specific electrical protection and monitoring. Typical project scope spans rated voltages up to 1000 V AC and busbar rated currents that are project-specific (commonly up to 4,000 A for heavy process panels) with short-circuit withstand ratings selectable from ~25 kA to 120 kA (symmetrical) depending on busbar dimensions, bolted joint treatment and fault- making devices. Designs reference IEC 61439-1/-2 for assembly verification, IEC 60947 series for switchgear and controlgear, IEC 60079 when flammable solvents are present, IEC 61000 for EMC, and IP requirements per IEC 60529. Pharma panels are built to support GMP (EU GMP Annex 1), ISO 14644 cleanroom classifications and FDA/EMA validation protocols (IQ/OQ/PQ). Mechanical construction uses stainless steel 316L enclosures, electropolished or passivated finishes, rounded corners and flush doors for cleanability; options include mirror-polished faces, hygienic cable entries, and sealed gland plates to maintain ISO Class requirements. Typical enclosure ratings range IP20 (controlled plant rooms) to IP66 (washdown and containment areas); ATEX-certified variants follow IEC 60079 for solvent-handling zones. Functionally, custom panels integrate MCC (motor control centers), PCC (power control centers), soft-starter and VFD clusters, UPS and ATS systems, harmonic filtering, and local control HMI/SCADA gateways. Product-level examples for modular switchgear form factors include Siemens SIVACON and MNS families and Schneider Electric Prisma Set or Harmony HMI solutions when OEM-style configurations are required. Communication architectures use Profinet, EtherNet/IP, Modbus TCP, or OPC UA with industry-grade PLCs; for regulated records, electronic access and logging consider 21 CFR Part 11 requirements. Electrical segregation is designed per Forms of Separation (Form 1–4b as required) with selectable segregation between busbar, cable compartments and functional units. Protection schemes include selective overcurrent (IEC 60947-2/4), earth-fault and residual current monitoring, differential protection for critical trains, and arc-flash mitigation (arc-resistant construction and fast fault clearing). Verification includes type tests and routine tests per IEC 61439 (temperature-rise, dielectric, short-circuit verification, IP testing) plus factory acceptance testing (FAT) and site SAT; deliverables include assembly certificates, verification reports and traceable component datasheets for validation files. For pharmaceutical integrators and EPCs, custom engineered IEC 61439 panels deliver repeatable electrical performance, hygienic construction, validation documentation and third-party testing options to meet regulatory scrutiny while integrating modern power and control technology into cleanroom and production environments.
Key Features
- Multi-function integration in a single lineup
- Non-standard ratings and form factors
- Special environmental ratings (IP65, ATEX, marine)
- Custom HMI and operator interfaces
- Designed for pharmaceuticals operating environments
- Industry-specific protection and monitoring requirements
Technical Specifications
| Rated Current (InA) | Project-specific |
| Short-Circuit Rating | Project-specific |
| Rated Voltage | Up to 1000V AC |
| Form of Separation | Form 1–4b |
| IP Protection | IP20–IP66 |
| IEC Standard | IEC 61439-1/2 |
| Target Industry | Pharmaceuticals |
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