Ingeniería enfocada en cero paros no programados y entrega 100% lista para auditoría. Eliminamos brechas de coordinación y órdenes de cambio costosas mediante cumplimiento dual NOM-001 y NEC 2023.
Medical Devices
General Contractor
Electrical Contractor
Medical
Medical Devices
Medical Devices
Cleanroom Contractor
Medical Devices
General Contractor
Electrical Contractor
Medical
Medical Devices
Medical Devices
Cleanroom Contractor
Design and construction of Cleanrooms with ISO 14644 certification for high-demand sectors: pharmaceutical, aerospace, and advanced manufacturing. We execute conventional, modular, hybrid solutions, and USP 797 labs, integrating certification and validation from concept to commissioning with audit-ready documentation at startup.
→ Explore Cleanroom Services → Request Technical ReviewIntegrated power engineering from the Medium Voltage (MV) service entrance to the final Low Voltage (LV) branch circuits. We design and execute the complete electrical lifecycle: MV substations, high-capacity 480V distribution for industrial loads, and precision downstream infrastructure for 110V/220V critical services. Our systems are engineered for zero-defect startup and future-proof scalability.
→ Explore Industrial Power → Request Technical ReviewIndustrial infrastructure and build-outs: structural steel, concrete foundations, elevated slabs, and architectural finishes for manufacturing plants. Full MEP coordination under the Design-Build model, eliminating trade gaps and ensuring turnkey delivery.
→ Explore Industrial Build-Out → Request Technical ReviewApplied electrical engineering: short-circuit, load flow, and coordination studies in ETAP / SKM. Power quality analysis and Arc Flash risk assessment per NFPA 70E, delivering stamped engineering packages for UVIE dictum and CFE approval.
Regulatory path management: UVIE electrical dictum, CFE interconnection, FDA 21 CFR Part 11 compliance, ISO 14644 classification, and AS9100 audits. We deliver audit-ready documentation that satisfies both Mexican authorities and global compliance teams.
Preventive and corrective maintenance for cleanrooms and mission-critical infrastructure. Dedicated 24/7 emergency response to minimize unplanned downtime for high-availability industrial facilities across the border region.
POR QUÉ ACTUAR AHORA
$150,000–$500,000 USD / evento
Línea parada, producto rechazado, penalizaciones de cliente. Una subestación comisionada correctamente elimina este riesgo.
→ Potencia Industrial con CFE-ready en 16 semanas
Auditoría FDA fallida = paro total de línea
Un hallazgo crítico en FDA 21 CFR 820 puede detener producción por semanas. IQ/OQ/PQ documentado desde construcción previene el riesgo.
→ Cleanroom ISO con certificación incluida
+30% tiempo · responsabilidades fragmentadas
Cuando arquitectura, MEP y construcción tienen contratos separados, los retrasos no tienen dueño. Design-Build elimina ese riesgo desde el día uno.
→ Design-Build: un contrato, un responsable
Weekly briefings on cleanrooms, electrical infrastructure, and manufacturing across Northwest Mexico.
An FDA warning letter to Optikem International exposes a critical blind spot: a cleanroom that passed ISO 13485 certification but was never recertified. HEPA filters degrade silently — ISO Class 7 environments drift out of specification within 18 to 36 months without a structured requalification program.
Common nitrile and latex gloves shed stearate particles nearly identical to microplastics — potentially inflating contamination counts and compromising regulatory data across industrial cleanroom operations.
Mexico's Sheinbaum administration unveiled a US$22.3 billion program adding 22+ GW via 51 CFE-led projects. Power availability, pricing and contract structures will be increasingly shaped by CFE's investment calendar.
Revisión de ingeniería directa. Sin intermediarios de ventas. 48-hour response time.
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