MD Compliance Ltd is a medical devices regulatory and quality management systems consulting company based in the United Kingdom.  We provide regulatory compliance consulting to customers based in any country.  Our services are focused on compliance with EU, UK, USA and Canadian regulatory requirements, including MDR, FDA and Health Canada submissions such as Technical Documentation, 510(k) compilations and submission, Canadian MDL applications, and more.  We are specialists at QMS support, including all aspects of ISO 13485, 21 CFR Part 820 and MDSAP, and we are ready to perform internal audits, mock audits / mock inspections, and external audit remediation.

MD Compliance

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