Mindy McCann
VP Regulatory Compliance, Qserve Group, USA
![](https://rmd2022.com/wp-content/uploads/sites/62/2020/12/Mindy-McCann.jpg)
Mindy has multi-faceted medical device regulatory experience, having worked for a start-up, large global company and two notified bodies before joining Qserve, a medical device consulting company Mindy’s hands-on experience as a development engineer, notified body auditor and technical file reviewer, global certification manager, and executive has led to a practical approach in developing and implementing regulatory, quality and clinical strategies and supporting documentation.