AES Cleanroom Technology helps life sciences companies bring their ideas to life in a fast and safe way. Whether you’re scaling biotech production, manufacturing critical therapies, or advancing diagnostics, we provide cleanroom systems that perform to the highest standards in compliance, control, and cleanliness.
AES has transformed the landscape of modular cleanroom design, manufacturing and construction. What began as a vision to elevate industry standards has evolved into a legacy of cleanroom solutions that protect the world’s most critical processes.
Our journey is powered by a simple belief: exceptional environments enable extraordinary outcomes.
Precision and cleanliness are non-negotiable for medical device manufacturing. AES designs and installs cleanroom systems for Class I, II, and III devices, which support everything from sterile packaging lines to implantable assemblies. Our ISO 7 and ISO 8 compliant spaces are engineered for FDA 21 CFR Part 820 alignment and are adaptable to changes such as robotic integration and multi-product workflows.
AES cleanrooms play a vital role in the production of diagnostics and molecular testing platforms, which include PCR, antigen, and antibody tests. These cleanroom environments are built for contamination control and traceability, which ensures that every test is accurate and reliable. Our cleanrooms provide the scalable foundation that diagnostics manufacturers need to stay ahead in the public health sector.
Research and development is the heart of life sciences innovation, which is why AES provides modular cleanroom solutions that let teams iterate freely and scale as needed. From private-sector hubs to academic labs, AES systems support environments for preclinical research and early-phase process development. Our modular approach lets R&D facilities evolve with new equipment and funding without requiring a complete rebuild.
AES Cleanroom Technology supports all clinical-stage manufacturers with the perfectly sized cleanroom environment for Phase I-III production. Our facilities are engineered for small-batch and high-quality outputs under strict GMP guidelines, providing flexibility for process changes and regulatory filings such as INDs or NDAs. We help clinical-stage companies transition from trial prep to market readiness, no matter the deadline.
We engineer specialized cleanrooms for compounding pharmacies that require precisely controlled environments for sterile and non-sterile medication preparation. Our facilities are designed for custom formulations and patient-specific dosing under strict USP guidelines, providing the flexibility needed for diverse compounding requirements and regulatory compliance. We help pharmacies deliver safe, high-quality custom medications while meeting evolving industry standards and patient demands.