McBride Compliance and Quality is the leading supplier of Software Quality Assurance and Regulatory Advice to industry and academia. Leveraging Jeff McBride’s vast experience in FDA, EMA, & MHRA regulated life sciences industries in the UK, Ireland, US, Far East and Mainland Europe.

McBrideCQ is the foremost provider of Software Quality Assurance to the emerging digital healthcare industry as a one stop shop solution to companies who seek to have medical devices that are solely/predominantly software through registration for CE Mark or FDA approval.

McBrideCQ can be the ‘Independent Quality Unit’ that you will require by the regulations and will represent your business/products in all dealings with any regulatory agency. We offer total solutions for CE Mark/FDA registration requirements.

Get in touch with us today to discuss your requirements for CE Marking medical devices and we can see how we can help you.