Cleanroom Solutions.
Angstrom Technology design, build and validate industry-leading critical environments. From Custom-built to Ready-to-ship, our range of cleanroom solutions will provide you with the most appropriate controlled environment for your process.
Our cleanroom solutions
Compare our cleanrooms and services to find the most appropriate solution for you.
Custom-built GMP cleanrooms
- Diminishes the risks inherent to (bio)pharmaceutical production.
- Protects against viable and non-viable particulates, as well as cross-contamination.
Custom-built ISO cleanrooms
- A repeatable environment for production of a reliable product.
- High-performance cleanrooms designed to interface with your existing facility.
GMP Consultancy Services
- Our GMP Consultancy Services are designed to support cleanroom users in navigating the complexities of Good Manufacturing Practice (GMP) requirements.
What sets us apart?
With an end-to-end service, our multidisciplinary team design, deliver, and commission complete cleanroom systems.
- Full project management and ongoing maintenance
- Decades of experience in functional and mechanical system design
- Technical specification and reliability of our cleanrooms is second to none
With a UK network of offices, we are ideally placed to support customers across the country.
Our success stories
We apply creative thinking to modular cleanroom projects, resulting in functional spaces that achieve a significant return on investment. Learn how we add value to our clients through our case studies.
You'll be in good company
Frequently asked questions
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.
