Does Zetron’s system comply with international pharmaceutical industry standards?

Yes, Zetron's environmental monitoring systems fully comply with major international pharmaceutical industry standards and regulatory requirements, supporting global GMP compliance and cleanroom management for pharmaceutical and biotech operations.

• Compliance with Authoritative International Standards: Our systems meet EU GMP Annex 1 (2022) for sterile manufacturing, US FDA 21 CFR Part 11 for electronic records and signatures, ISO 14644‑1:2015 for cleanroom air cleanliness classification, and the global Pharmacopoeia requirements for environmental control.
• 24/7 Real-Time Environmental Monitoring: The system provides round‑the‑clock monitoring of airborne particles, viable microorganisms, temperature, humidity, differential pressure, and other critical parameters, ensuring stable production environments.

This robust compliance framework enables customers to meet stringent global regulatory requirements, mitigate compliance risks, and maintain consistent product quality and safety.