Phillip Yan
Manager of Quality Assurance
Phillip has spent his career in medical devices as a quality assurance and compliance specialist, supporting product development, regulatory submissions, and quality management systems for both startups and large multinational corporations. He brings to Triple Ring deep expertise in regulatory compliance, with a focus on U.S. FDA regulations, ISO 13485:2016, MDSAP, EU-MDR, and UKCA requirements.
Prior to joining Triple Ring, Phillip held key quality and regulatory roles across a range of medical device companies. He has earned certifications including Regulatory Affairs Certificate (RAC), ASQ Certified Quality Auditor, ISO 13485:2016 Lead Auditor, and EU-MDR and MDSAP Auditor.
Phillip earned a B.S. in Biomedical Engineering from the University of California, Irvine.
Let’s solve hard problems together.
Triple Ring is a co-development company. We stand side-by-side with innovators and entrepreneurs to solve hard problems, launch breakthrough products, and create new businesses.