InSpecTM Product Range

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InSpecTM is a range of water and alcohol based rotational disinfectants designed to meet current rules and guidelines from pharmaceutical regulators.

InSpecTM DE 

Popular Cleanroom disinfectant. Ethanol safely denatured with 5% IPA.

InSpecTM DE is a sterile preparation of 70% denatured ethanol (DE) in 30% Water For Injection (WFI) quality water.

These products are supplied sterile, double bagged, gamma irradiated and provided with certificates of analysis, irradiation, sterility and endotoxin level.  

InSpecTM DE is available in a 5L screw capped container, a 1L trigger spray or a 500ml trigger spray. The trigger spray bottle is designed to prevent contamination of the product with micro-organisms such as bacterial spores which can survive in 70% alcohol. The trigger spray bottle has a validated in-use shelf life.  

InSpecTM DEis also available in 15pc and 50pc session wipes as well as 200pc tub wipes.  

InSpecTM DE is manufactured in an ISO 6 Cleanroom, filled under an ISO 5 localised air shower in the ISO 6 background. Batch certified covering areas such as analysis, sterility, endotoxin and irradiation dose. Manufactured to GMP under an ISO 9001 quality system.

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Technical Specifications

A full technical file providing product efficacy, shelf life studies, microbial data and sterilisation validation data is available on request to those customers requiring this level of detail.

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Request a quote

Call our team on U.K. 0845 0739529, International +44 (0) 1527 830942 or fill in the form below, and we will be in touch at the earliest opportunity:


The disinfectants used should have proven efficacy:

The InSpecTM range passes all the appropriate EN standards EN1276, EN1650, EN13697 and EN13704. Thus the decision to move to a validation programme is met with a level of assurance that the disinfectants will work.

Our formulations are fixed:

The formulations of our products are fixed and will not change unless through circumstances beyond our control. This means the cost of revalidating a disinfectant due to formulation change is minimised.

Registered under the BPD:

All of our biocides are registered under the BPD (Biocidal Products Directive) thus the validation effort will not be in vain. Products validated today will be available for many years to come. 

Full Traceability:

We formulate and source our products from a variety of leading suppliers in Europe. Our alcohols come from leading UK suppliers, offering full traceability.

Uses water manufactured to WFI quality:

Where solutions are required at in-use strength the InSpecTM range uses water manufactured to WFI quality. Thus the risk from endotoxin is controlled and the water quality should always match or exceed that which is available in the Cleanroom.

We minimise particulate and bioburden contamination during processing:

The products are manufactured within an ISO 6 Cleanroom environment and filled under an ISO 5 localised air shower. Additionally all products will be filtered prior to fill through a 0.2 micron filter. This means our critical manufacturing procedure matches industry expectations, minimising particulate and bioburden contamination during processing and ensuring clean product and a successful terminal sterilisation process. 

Exceptional Water Quality:

Our Contamination Control Products are built around an exceptional water quality system, fully validated and generating WFI quality water for blending on demand and piped directly into our Class 6 Cleanroom.

Sterile Content and Packaging:

The main terminal sterilisation method is a validated gamma irradiation procedure using a minimum of 25kGy affording a SAL of 10-6. Thus there is a very high level of confidence that the product content and packaging are sterile.

Multiple bagged:

All products will be multiple bagged to allow smooth transfer into the Cleanroom minimising the risk of contamination being carried into your Cleanroom. 

Speed up Quality Acceptance Procedures:

All batches of product will be supplied with appropriate certificates of analysis, irradiation, sterility and endotoxin speeding up quality acceptance procedures. 

Defined using Pharmaceutical Specified Methods:

Critical parameters such as shelf life and in-use shelf life are defined and determined using pharmaceutically specified methods.