Speaking Engagements

Regulation of In Vitro Diagnostics as Medical Devices

June 8, 2018
Washington, District of Columbia


Steven Tjoe was a featured speaker on FDA’s regulation of in vitro diagnostics as medical devices at the Food and Drug Law Institute (FDLI), New to Food and Drug Law Group.  Topics addressed included the unique regulatory and policy considerations applicable to laboratory developers, the field of precision medicine, and the diagnostics industry at large.