A dual-qualified professional in engineering and law, Mr. Louis-Paul Marin has developed distinctive expertise at the intersection of technology and regulatory frameworks. This unique combination enables him to gain an in-depth understanding of product design, manufacturing processes, and quality assurance, while also mastering the complex and constantly evolving compliance requirements and regulatory frameworks governing the medical device industry.

Specializing in regulatory affairs, Mr. Marin supports companies in interpreting and applying international medical device safety requirements, as well as in drafting and negotiating strategic agreements essential to their business relationships (quality agreements, distribution and manufacturing contracts, collaboration agreements, research contracts, etc.).

He stands out for his ability to secure market access and support the maintenance of regulatory authorizations across multiple jurisdictions. Throughout his career, Mr. Marin has contributed to the approval of numerous medical devices in Canada, the United States, and abroad, and joined a leading law firm partnership after only a few years of practice.

He is also actively involved as a speaker and invited expert, serves as a board member, and works as a university lecturer and trainer.