The demand for qualified regulatory professionals in the medical device industry has always been strong. And demand continues to grow, fueled by ever-evolving laws and regulations in the US and worldwide.
The Master of Science Program in Regulatory Affairs and Services (RAS) focuses on medical devices and provides depth on FDA and international regulatory requirements and procedures for medical devices that other Master’s Programs cannot match. Courses are taught be industry experts and are applications oriented. RAS Program graduates are working in medical device companies, large and small, CROs and FDA.
Hear what Mark Duval a nationally recognized expert in Regulatory Affairs has to say about the RAS Program.
Apply now for the fall 2014 RAS student cohort. The RAS Program has broad applicability for the US medical device industry and applications are being accepted both locally and nationally. Remote students can connect synchronously to classes via Adobe Connect.
Is the RAS Program and a career in medical device regulatory affairs right for you? Click on the questions below for additional information.
2013-14 Brochure (pdf)