For example, a client outside of Europe wants to improve their CSSDs / Sterile Processing and also demonstrate they meet best international practices and standards.

EUsterile engineers and consultants will liaise with the responsible persons and begin with an initial audit of several CSSDs and their installed equipment.

Reviewing standards, guidance and local policies allows us to get a snapshot of where there may be gaps and opportunities for improvement.

Equipment audit and user interview will identify issues such as wet autoclave loads and we advise the necessary corrective actions.

We develop a standardised test regime that can be carried out weekly, quarterly and annually throughout the region to demonstrate that performance requirements are being consistently met.

We then oversee and/or manage validation activities on behalf of the client. Lastly we review the reports and test results, providing ongoing advice, feedback and ultimately satisfactory sign off.

Impartial advice is provided year round on all matters from equipment purchasing to department design.

We provide independent expert technical advice on all decontamination matters from writing new equipment specifications to interpreting validation results on existing equipment.

We audit CSSDs / Sterile Processing processes across many areas such as ‘sterilisation engineering plant’ to device ‘packing’ or ‘transportation’.

We assist the hospital with cycle optimisation; working together to continuously improve.

Our Authorising Engineer (Decontamination) AE(D) is our sterilisation consultant who will review validation reports carried out by third parties and provide ongoing advice, feedback and ultimately satisfactory sign off. Impartial advice is provided year round