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Get in touch

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Thank you for your enquiry to STERIS Instrument Management Services. We aim to respond to all enquiries within 1 working day. If your enquiry requires a more in-depth response, we will still respond to notify of that.

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Quality & Governance

Quality & Compliance

Quality is the very core of everything we do at STERIS Instrument Management Services.

Our comprehensive internal quality management system ensures compliance to BS EN ISO 13485 and applicable legislative requirements. We know that the services and products we supply are crucial to patient safety and therefore we never stop seeking excellence in quality through continuous improvement initiatives.

Our commitment to compliance and improvements is integral to our business and the sector in which we operate 

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A passion for quality

Request Quality certificates for any of our sites

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Our leadership team

At STERIS, we help our Customers create a healthier and safer world

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Sustainability

At STERIS, we are dedicated to make a positive impact on the world around us

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Global Overview

STERIS global headquarters are based in Mentor Ohio, USA providing healthcare solutions globally

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Governance Structure

STERIS Instrument Management Services complies with the requirements of the Medical Device directive and BS EN ISO 13485.

STERIS Instrument Management Services are dedicated to improving patient care and safety. To ensure continuous improvement, STERIS works towards national best practice guidance recommendations and monitors the market for technical and scientifically valid innovations which can improve the products and services we provide to our customers.

In the United Kingdom, the national competent authority is the MHRA and our accredited notified body is Intertek.