Pharmaceutical and life-science facilities demand classified cleanrooms, validated systems and audit-ready documentation. Here is how a turnkey design-build partner delivers GMP-grade environments in Mexico.
Classified, GMP-grade cleanrooms
We design and build ISO 14644 classified cleanrooms with the wall and ceiling panel systems, HEPA filtration, pressurization cascade, epoxy/coved flooring, air showers and pass-throughs that GMP environments require.
HVAC and clean utilities
- Precision temperature and humidity control
- Filtration, pressurization and airflow design
- Clean utilities, purified water and process services
- Electrical capacity and backup, with CFE on the critical path
Validation and documentation
We deliver IQ/OQ, particle counts, airflow and pressure testing, and a GMP-ready documentation package — so your facility passes COFEPRIS and customer audits.
Compliance, local and international
Mexican norms (NOM, COFEPRIS, STPS) and international standards (ISO, NFPA, ASHRAE, GMP) are integrated from the design stage, not retrofitted.
One accountable team
Cleanroom, HVAC, utilities and validation interact tightly. CTECP delivers them under one design-build / EPC contract — 250+ projects, 580,000+ m², trilingual team, USD 20M+ bonding.