This club was created to bring together regulatory professionals to discuss all areas of the medical device product lifecycle. 

Our goal is to share our knowledge with one another, network, learn from the experiences of those who walked this path longest and educate the future regulatory professionals. 

Our topics include but are not limited to: Device Classifications, Quality Management Systems(QMS), Clinical and Non-clinical Studies, Regulatory Pathways, Good Manufacturing Practice (GMP), and much more. 
