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About Constant Medical
Bringing world-changing medical innovations to life, from compliance to commercialization
Professional Team
Our team brings together extensive experience in regulatory compliance, quality management systems, product registration, market access strategy, and commercialization across multiple jurisdictions. By combining global expertise with local regulatory insight, we help our clients efficiently achieve compliance, accelerate market entry, and maintain sustainable business success throughout the product lifecycle.
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Years
Our core team consists of seasoned international experts with more than 15 years of experience.
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Regions
Guangzhou (Headquarters) | Hong Kong (International Hub) | Shenzhen / Suzhou / Hefei / Foshan (Industrial Clusters)
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Major Markets
China (NMPA) · Europe (CE) · North America (FDA) · South America (ANVISA) · Asia-Pacific (PMDA/TGA)
Medphoenix Group Structure
Meet our professional team
Mr. Tim DENG
Deputy General Manager
With over 15 years of medical device CRO leadership, Tim has served as a top-tier firm’s Head of Marketing and Sales Director. He actively contributed to China’s MAH policy advancement and spearheaded the registration of the nation’s first medical-grade wearable device. Tim has delivered end-to-end product registration and global market access strategies for over 100 industry leaders, including MicroPort, Mindray, and GE Healthcare.
Dr. Sophia Lam
General Manager
Leveraging a PhD in Life Sciences, an Honorary Research Assistant Professorship at HKU, and over 15 years of medtech research expertise, I excel in driving regulatory submissions across Southeast Asia and leading high-performing teams to secure major non-dilutive funding, including the INCU-BIO incubation program and three consecutive top placements in the USTP, while maintaining active credentials as an ASQ Registered Medical Device Auditor.
Mr. Kenmok Mok
Operations Director
A seasoned biomedical engineering expert with over 25 years of medical device industry experience, this professional specializes in design development, R&D, and global CDMO operations. Backed by certified ISO 13485 and ASQ auditing credentials, they excel at building audit-ready quality management systems from the ground up. As a trusted consultant for cross-border market expansions, they seamlessly steer successful medical device registrations and compliance frameworks across Asia.