Unlocking Success: Quality, Compliance, and Commercialization in MedTech
Join us for the Regulatory Affairs Professionals Society (RAPS) & Life Sciences Week event, where we’ll dive into regulatory compliance and early commercialization strategies for startups in Medical Devices, Diagnostics, and Digital Health.
Becki Hiebert, Principal Consultant at BH Quality Management Consulting, will present "RAPS, Regulatory Affairs, and MedTech Startups," offering practical guidance on navigating regulatory hurdles and leveraging compliance as a competitive edge.
Our keynote speaker, Dr. Solomon Ssenyange, PhD, Co-Founder of RedNOx, Inc., will share "An Entrepreneurial Journey: A Silicon Valley Success Story," revealing valuable lessons from his own experiences building and scaling a successful startup.
Following the expert presentations, join us for a dynamic panel discussion, “From Concepts to Market: Overcoming Early Challenges and Strategies for Successful Medical Device Commercialization.” Moderated by Brian Lewis, President of Brian Lewis and Associates Inc. and Director of Industry and Investor Relations at Excite International, this session will feature insights from top industry leaders and innovators.
Panelists include Dr. Robert Paproski, Chief Technology Officer at Nanostics, Dr. Rajan Gupta, COO of NanoSpeed Diagnostics Inc., Dr. Amit Monga, Executive in Residence at API and Investor, and Rhiannon Adams, Partner and Head of the Intellectual Property Group at Parlee McLaws LLP. Together, they will share their experiences in overcoming sector-specific challenges, achieving quality-driven success, and understanding what investors look for in thriving startups.
Following the event, join us for a networking reception, sponsored by Parlee McLaws LLP, from 4:00 to 6:00 PM. This is a great opportunity to connect with peers and industry experts, fostering meaningful conversations to support your growth in the Medical Devices, Diagnostics, and Digital Health sectors
Event note; in-person capacity is at 100 individuals. Guests who register after the cap has been made can participate via a hybrid model. A link will be sent to those guests prior to the event.
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Sector: Medical Devices, Diagnostics/IVDs, Digital Health/SaMD/AI
Professional Interest: Compliance, Quality Assurance and Control; Product Development