Welcome to BIOMEDevice Silicon Valley 2023 Registration
BIOMEDevice Silicon Valley brings engineers, business leaders, disruptive companies, and innovative thinkers from the region’s top start-ups and medical device OEMs together to inspire the next life-changing medical device.
Conference Registration and Pass Selection
Expo Pass
Conference Pass
Master Class Conference Series
Day 1: Start-Up SeriesWelcome to our Master Class Series for MedTech Start-Up Companies! This educational program is designed to provide medtech entrepreneurs with the knowledge and skills they need to succeed in the highly competitive and ever-evolving world of medical technology. Throughout this series, you will learn from experienced professionals and industry leaders who have successfully navigated the challenges of bringing a new medical device or technology to market. You will gain valuable insights into everything from product development and regulatory compliance to marketing and sales strategies. Day 2: Design & Development SeriesThis Master Class Series will provide you with a deep understanding of the medical device design and development process, as well as the tools and techniques needed to bring your innovative ideas to life. Throughout this series, you will learn from experienced professionals and industry leaders who have successfully navigated the challenges of medical device design and development. You will also have the opportunity to network with other professionals in the field, and gain valuable insights into the latest trends and developments. Whether you are just starting out in the field of medical device design and development or are looking to take your career to the next level, our program will provide you with the knowledge and skills you need to succeed. Day 2: Policy & Regulation SeriesBIOMEDevice is teaming up with MEDIcept to bring you the Master Class Policy & Regulation Series. Throughout this series our expert instructors will cover a range of topics critical to navigating the regulatory landscape. Topics will include; understanding the regulatory framework for medical devices in the US and internationally, navigating the regulatory pathways for FDA approval, conducting clinical trials and obtaining necessary data, developing a regulatory strategy and submitting a successful application, navigating post-market surveillance and reporting requirements, and understanding the impact of emerging technologies and trends on regulatory policies. *Students enrolled in a medtech or engineering program and Start-ups who are in early thru late-stage funding qualify for our Start-up & Student Rate. Students and Start-ups registration will be verified and are subject to Show Management determination and approval.
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To modify an existing registration click here Exhibiting? The primary contact for your company received an email to log in to your Exhibitor Dashboard to register staff. If you are unable to complete your registration, BIOMEDevice Silicon Valley 2023 will contact you by email and retain your details so that you can pick up where you left off.  Registration Help
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