About C-Pro Direct
C-Pro Direct has been supporting children, families and clinicians affected by Clubfoot since 2005.
|About C-Pro Direct
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).
|ISO 13485 Certificate
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.
Support to the Global Clubfoot Community
C-Pro Direct supports Clubfoot charities, children and families with special needs and scientific research into Clubfoot.
|Charities we Support