At Steeper we pride ourselves on our dedication to our customers, and this includes our commitment to industry-leading testing and quality standards. Over recent years, we have invested significantly in testing technology, procedures and standards, and in 2021, we successfully completed the transition to ISO 13485: 2016 and the Medical Devices Signle Audit Program (MDSAP) certification for the manufacture of prosthetic and orthotic devices.

The ISO 13485 and MDSAP certifications are globally recognised and demonstrate our excellence in quality management and best practice throughout the design, manufacture and supply of safety assured medical devices.

Steeper Group are also ISO 9001: 2015 certified which further illustartes our commitment to provide excellence in customer services and consistency across our prosthetics, orthotics and assistive technology product portfolios and services provision.

To request a copy of our Quality Policy, please click here.

Further Standards and Accreditations

Steeper is accredited to the following standards: ISO 9001: 2015, ISO 27001: 2013, ISO14001:2015, ISO50001: 2011, Investors in People, Disability Confident Employer, BHTA and TRI approved, FDA and MHRA registered. As a medical device manufacturer, Steeper also comply with requirements of the Medical Devices Regulation (EU) 2017/745.

For more information on the Modern Slavery and Human Trafficking Act, please click here to view the Steeper Group Statement.

For further information on our accreditations, certifications and policies, please contact us at enquiries@steepergroup.com.