Qualified as a Manufacturing Systems Engineer, I gained a wide engineering experience as a Production / Industrial Engineer, Production Manager and Quality Assurance Manager in the UK. Arrived in France in 1996, gained experience as a QA Manager, specialising as a Regulatory Affairs Manager for both medical device and in-vitro device manufacturers. In 2006, I created C-REG Medical : a Complete REGulatory Affairs Service. Fluent in French & English, I assist small medical device manufacturers in their Regulatory obligations to your requirements, for both Europe and the USA. Please feel free to consult the website : www.c-reg-medical.com