- Cleanroom Certification
Certified Excellence in Cleanroom Validation
Comprehensive cleanroom certification ensuring your pharmaceutical, medical device, and biotechnology facilities meet the highest industry standards and regulatory compliance requirements.
- Certification Process & Standards
Our Rigorous Certification Standards
At Aeris Validation Services, we follow FDA, USP, and ISO standards to ensure your cleanroom environment maintains the strictest quality protocols. Our certified technicians conduct comprehensive inspections and advanced testing protocols to measure environmental conditions including particulate levels, air pressure differentials, temperature, humidity, and microbial contamination. We provide detailed documentation that satisfies regulatory audits and maintains your facility’s operational integrity. With 500+ facilities certified and a 99.8% compliance rate, our validation process is designed to minimize downtime while delivering thorough, audit-ready results.
Your Trusted Partner in Validation Excellence
Comprehensive cleanroom certification and equipment validation ensuring safety, quality, and regulatory compliance for critical pharmaceutical and medical facilities.
- Timeline & Efficiency
Turnaround Without Compromising Quality
We understand that facility downtime costs money and impacts productivity. That’s why our streamlined certification process delivers results quickly without sacrificing thoroughness. Initial cleanroom certification typically takes 2-4 weeks from consultation to final documentation, with smaller facilities completing in 1-2 weeks and larger pharmaceutical operations in 4-6 weeks. Our 24/7 support team provides rapid response times for urgent certification needs, and we maintain complete documentation with detailed reports and compliance certificates ready for your next inspection.
Get Trusted
Validation Experts,
Process Made
Simple
- Partnership & Support
Your Complete Validation Partner