We are specialized in meeting the requirements of pharmaceutical and medical cleanrooms, whose needs are often very different from those of electronics cleanrooms.
With a reputation for innovation, proven by awards from the cleanroom industry, we offer technical expertise and extensive processing capability.
Due to several Grade B, C and D cleanrooms at state-of-the-art manufacturing facilities in Wales, the facilities are continually expanding and upgrading to meet the latest GMP recommendations and maintain the highest possible standards of manufacture.
Our extensive technical support includes specialist testing and quality laboratories, which operate to the principles of Good Laboratory Practice. As well as testing and evaluating every stage of the production cycle, in-house validation testing can be offered to your customers.
We support them with their own validation processes through the supply of comprehensive technical information, including both in-house and independent test data.
Confidentiality, expertise and high levels of technical support are available throughout all stages of the specification and validation process.
Awarded BS EN ISO 9001:2000 and BS EN ISO 13485:2003, we hold the Medical Device Directive 93/42/EEC for the design, manufacture and distribution of sterile and non-sterile cleanroom products.
We keep abreast of new legislation and regulations and we are committed to taking our biocide range through the Biocidal Product Directive registration process.
The sterile manufacturing facilities are regularly audited by major pharmaceutical companies worldwide, who themselves hold GMP accreditation, as well as by the UK National Health Service and private hospitals.