Cleanroom engineering is a technical and specialized process that enables the design, construction, and validation of controlled environments where minimal particle presence and highly regulated atmospheric conditions are required. These facilities are essential in sectors such as pharmaceuticals, biotechnology, food production, microelectronics, and research laboratories.
At IS CLEAN ROOMS, we understand that every cleanroom project is unique. That’s why we approach each installation through three key phases:
| Engineering Phase | Main Objective | Key Deliverables |
| Conceptual Design | Define requirements and assess project feasibility | User requirements, functional diagram, preliminary cost estimate |
| Basic Design | Translate the concept into an initial technical solution | Layouts, main systems, cost estimate |
| Detailed Design | Prepare all documentation for construction | Construction drawings, technical specifications, validation plan |
With a specialized technical approach and over 15 years of experience designing critical environments, IS CLEAN ROOMS supports its clients at every stage—from defining functional requirements to delivering a cleanroom that complies with GMP, ISO 14644, and FDA standards.
At IS CLEAN ROOMS, we specialize in the design, manufacturing, and commissioning of cleanroom projects. Our technical approach is based on precision, efficiency, and strict regulatory compliance, allowing us to create optimal environments for sensitive and highly regulated processes. Each solution is tailor-made to ensure the environmental control required in sectors where air quality and sterility are essential.
