Background

C-Pro Direct has been supporting children, families and clinicians affected by Clubfoot since 2005.

Commitment to Quality and Regulatory Compliance

C-Pro Direct operations are externally accredited to ISO 13485 (medical device manufacture).  The companies products conform to the European Medical Device Regulation (MDR 2017/745) and so are "CE" marked and the UK MDR (SI 2002 No: 618) and so carry the "UKCA" marking.  Our products are also registered with the US FDA and comply with all relevant US CFR regulations.

C-Pro Direct uses only the highest quality materials in the manufacture of its products and has demonstrated their suitability for use through the application of ISO 10993-1 Biological Evaluation of Medical Devices (material toxicity).

Commitment to the Environment and Socially Responsible Business

C-Pro Direct is committed to carbon neutral manufacturing and to achieving net zero by 2050.  We have achieved the Green Small Business accreditation and implemented an ISO 14001:2015 Environmental Management System (EMS).

C-Pro Direct has implemented measures to ensure both the business and its supply chain are and remain free from Modern Slavery and Human Trafficking.

Environmental Policy

Carbon Reduction Plan

Modern Slavery and Human Trafficking Policy

Support to the Global Clubfoot Community

C-Pro Direct supports Clubfoot charities, children and families with special needs and scientific research into Clubfoot.