Aseptic pharmac cleanroom facilities must meet a variety of industry standards, such as US Fed 209E, BS

5295, EU GMP (Good Manufacturing Practice), or BS EN ISO 14644-1 (1999). However, comparing these

standards can be challenging due to differences in conditions, sampling methods, pressure requirements,

and air change rates. Navigating these complexities requires expert guidence, and that’s where we come in.

With over 20 years of experience in providing specialist pharma cleaning and decontamination solutions, our

skilled and knowledgeable team is well-equiped to help you meet the required standards for your aseptic or

specialist pharma cleanroom.

The increasing prevalence of fungi, such as yeasts and molds, poses significant challenges for clean room

facilities. Although pathogenic varieties make up a small percentage of the known fungal species, any

presence of mold or yeast can contaminate specimens and products.

Fungal resistance to biocides varies widely among species, with molds being more resistant than yeasts and

considerably more so than bacteria. Our team of professionals knows how to choose the approrpriate

disinfectant to combat specific contaminants and preserve your clean room’s integrity.

We stay up-to-date with the latest micro-cleaning techniques and regulations, ensuring that your cleanroom

processes remain efficient and effective. Our services encompass a wide range of cleaning and

decontamination methods, catering to your specialized pharma cleaning needs and requirements.

We guarantee quality work and your complete satisfaction. Contact us today for a Decontamination Audit

and Evaluationto transform your cleanroom from merely clean to pristine.