Panel Sessions

As recognized knowledge leaders with many proven client successes, Ken Block Consulting (KBC) has been invited to participate in numerous industry conference panel sessions, covering topics from wireless device connectivity and 3D printing to US market entry and FDA regulatory strategy. These events include direct interaction with other panelists and audience members, allowing KBC to leverage our deep experience to help others who are seeking guidance. Co-panelists often include a mix of successful medtech entrepreneurs, regulatory attorneys, FDA employees, subject matter expert (SME) engineers, and others such as medical device reimbursement specialists.

Regulatory & Quality System Considerations for 3D Printed Medical Devices, RAPID + TCT, May 2019 [Detroit, Michigan]


Navigating the regulatory process, Med-Tech Innovation Expo, 2018 [Coventry, UK]


Today’s FDA and Go-to-Market strategies – U.S. and Abroad, Medical Device Resource Group, 2014 [Minneapolis, Minnesota]


Navigating the regulatory process, Mobile Medical Apps (MMA) Roadshow (co-sponsored with FDA), 2014 [Austin, Texas]


Medical Device Regulations in the US, Fukushima Innovation Beyond 3.11, 2013 [Fukushima, Japan]


Forecasting the future of the wireless medical device regulatory landscape, Wireless Connectivity in Medical Devices, 2013 [Munich, Germany]


US Regulatory Update, NTEC Mobile Health Series, 2012 [Frisco, Texas]


Premarket Pitfalls, Medical Devices Summit Midwest, 2012 [Minneapolis, Minnesota]


Regulatory: US & Europe, MedVentures Conference, 2012 [Frisco, Texas]