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About Us
AZ Technica was founded by Meghan McGovern and Celine Cohn in 2020. Meghan and Celine connected at the University of Arizona, where they both completed post secondary degrees.
As the medical device community in Arizona is tight knit, the two friends have been fortunate to get to work together several times over the years, during which they discovered their mutual respect for the role of compliance within the medical device industry.
When the opportunity presented itself to take a shot at striking out on their own, the two jumped in with enthusiasm and created AZ Technica.
Meghan McGovern, MS, RAC-US
Meghan McGovern, MS, RAC-US
Meghan McGovern, MS, RAC-US
Meghan McGovern earned her M.S. in Biomedical Engineering from the University of Arizona in 2014. Meghan has over 15 years of medical device industry experience in Engineering, Quality, and Regulatory with a broad range of device classifications, intended uses, and regulating bodies. Such devices have included class I respiratory devices
Meghan McGovern earned her M.S. in Biomedical Engineering from the University of Arizona in 2014. Meghan has over 15 years of medical device industry experience in Engineering, Quality, and Regulatory with a broad range of device classifications, intended uses, and regulating bodies. Such devices have included class I respiratory devices, class II gastrointestinal tubes, and class III cardiovascular devices. Meghan holds a regulatory affairs certificate in the US.
Celine Cohn, Ph.D.
Meghan McGovern, MS, RAC-US
Meghan McGovern, MS, RAC-US
Celine Cohn earned her Ph.D. in Biomedical Engineering from the University of Arizona in 2015. Celine has industry experience with class I and II respiratory devices and class III cardiovascular devices. Over the past few years, Celine has specialized in Quality Management Systems, the infrastructure in place with all medical device com
Celine Cohn earned her Ph.D. in Biomedical Engineering from the University of Arizona in 2015. Celine has industry experience with class I and II respiratory devices and class III cardiovascular devices. Over the past few years, Celine has specialized in Quality Management Systems, the infrastructure in place with all medical device companies that operate and sell in the global marketplace. Celine is a certified lead auditor for ISO 13485:2016.
About AZ Technica
