About C-Pro Direct
C-Pro Direct | |
Background 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).
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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.
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Support to the Global Clubfoot Community C-Pro Direct supports Clubfoot charities, children and families with special needs and scientific research into Clubfoot.
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Charities we Support |