Whether it is Pharmaceutical, Biotechnology, Engineering or Electronics the process requirements are the key and the cleanroom must always be designed to support the process.  Validair’s design approach will always result in a bespoke and individual design to suit the needs of each unique client requirement.

Validair understand that the development of cleanrooms demands the close co-ordination of building and engineering disciplines, with an understanding of the process requirements that will be conducted within the cleanroom.  A successful project delivery requires the application of multi-disciplinary skills and an appropriate selection of plant, equipment and cleanroom facility materials.

At Validair we work as an integral part of the client’s team from project conception to completion, providing valuable technical and engineering continuity through design and construction to qualification and facility validation.

In alliance with the customer’s team, we are ideally equipped to create and manage the following project specific design information:

• Preliminary & Detailed Design Phase Programmes
• Conceptual & Detailed Cleanroom Design Layouts
• Preliminary & Detailed Cleanroom & Equipment Capacities
• Preliminary & Detailed Facility & Equipment Specifications
• Order of Magnitude Budgets and Detailed Cost Estimates

Due consideration is given to CDM Regulations, Health and Safety, MHRA & FDA Requirements, ISO 14644, HTM Guidance Notes and all relevant industry guides.

Validair utilise the latest Cad software to produce detailed design drawings in 2D and 3D.  This allows a clear visual review of the coordination and integration between all service, utilities, process equipment and the cleanroom envelope.