We are a small, Client-focused group of skilled medical device professionals offering regulatory services (RaaS). Our Clients receive tailored, risk-based solutions to meet their individual needs. med-sherpa offers experts in the fields of quality, regulatory, clinical affairs, and project management. We offer turn-key solutions through our subject matter expertise & strategy augmented with project management, and individual contribution. While we specialize in US and EU medical device compliance we can also offer support for other major market regulation sets like Canada, Japan, and Australia.