Medical Device Playbook Newport Beach 2025
StarFish Medical is pleased to announce the return of Medical Device Playbook to Newport Beach, California on May 22, 2025.
Medical Device Playbook is one of North America’s largest MedTech events for entrepreneurial companies and medical device professionals. Designed to inform and inspire medtech and biotech entrepreneurs, Playbook brings you stories and insights from some of the industry’s most remarkable entrepreneurs and seasoned experts.
More details on Playbook Newport Beach 2025 will be announced soon.
Medical Device Playbook in-person events debuted in Vancouver in 2015, and Toronto in 2017 with the addition of Newport Beach in 2023. This fall we decided to introduce our first in-person event in Boston. Webinars continue along with live, in-person events in Newport Beach CA, Boston MA, Toronto and Vancouver.
“I travel all over the world and this conference was truly one of the most educational.”
Manny Villafaña, Founder of St. Jude Medical
Sponsorship Opportunities for Playbook Newport Beach 2025
Sponsorship opportunities are available. Contact Patrick Dean, StarFish Medical Director of Marketing, to discuss how your organization can gain visibility with the North American MedTech entrepreneur community.
About StarFish Medical
StarFish Medical provides award-winning design, development, commercialization, and flexible manufacturing outsourcing services —100% dedicated to the medical device and life science marketplace. StarFish Medical partners with innovative companies to create and manufacture breakthrough products for a full range of medical specialty areas including: Digital Health, Cardiovascular, Neurology, Urology, Gastroenterology, Otology, Ophthalmology, and In-Vitro Diagnostics.
StarFish Medical’s technical expertise includes electronics, mechanical, software/firmware systems engineering, in addition to industrial design and human factors. Regulatory Affairs (RA) and Quality Assurance (QA) consultants at StarFish Medical provide regulatory assistance for FDA, CE Mark and Health Canada submissions. Services include QA support for setting up QMS for start-up companies with implementation at the client’s site, and assisting with ISO 13485 certification audits.
For more information, contact: