The cleanroom design and build process
The cleanroom design and build process involves several critical steps to ensure the controlled environment meets the necessary cleanliness standards for specific applications, such as pharmaceuticals, electronics, and biotechnology. Here’s a breakdown of what the process looks like with Connect 2 Cleanrooms.
Introduction and discovery
Conceptual design
Detailed design
Specification development
Delivery and construction
Furniture fit-out
Our cleanroom range
Compare our cleanrooms to find the most appropriate solution for you.
ISO cleanrooms
- A repeatable environment for production of a reliable product.
- High-performance cleanrooms designed to interface with your existing facility.
GMP cleanrooms
- Diminishes the risks inherent to (bio)pharmaceutical production.
- Protects against viable and non-viable particulates, as well as cross-contamination.
Pre-designed
- A swift and cost-effective solution for a wide range of applications.
- Perfect for use as an entry-level solution or for a quick way to react to growing production demands.
Laminar Flow Cabinets
- Create an ISO class 5 – 8 enclosed environment using laminar airflow.
- Effectively reduce contamination in workspaces involving sensitive products.
Frequently asked questions
We offer softwall, hardwall, and monobloc systems as options for your cleanroom project. GMP cleanrooms will always need the flush panel system, but ISO cleanrooms are more flexible. The right construction type for you will depend on your process, but our Project Sales Engineers will be able to talk you through your options.
This depends on the construction type and class, but we can provide you with a rough order of magnitude (ROM) cost which gives you an estimated price range based on your requirements. Contact us to request your ROM price.
Every cleanroom design and build project will be validated during the commissioning phase. Then ISO 14644-2:2015 dictates that they need to be validated every 6-12 months depending on their class and your risk assessment. We have a dedicated after-sales and validations team who can talk you through your requirements.
Ultimately, this depends on your own process and risk assessment. If you aren’t sure, speak with your regulatory body and auditors to find out what their expectations are. We have a regulatory and governance team who will make sure your new cleanroom is designed to be compliant with your required ISO class or GMP grade.
Start a project with us
Our design and build specialists have experience working with customers in all kinds of industries on a global scale, achieving great results time and time again. We’d love to work with you as well!