Medical device testing guidance

The regulatory experts at Cranage Veritas can assist with all elements of medical device testing. We can help from the concept stage, through to gaining market access. Our medical device services includ: - Guidance and assistance with the Medical Device Regulations (EU 2017/745) - Article 15 Person Responsible for Regulatory Compliance. - FDA 510 (k) pre-market notification guidance - Assistance with CE marking Get in touch with our team to discuss your medical device testing and regulatory requirements

For more information on Medical device testing guidance talk to Cranage Veritas