About
Recognizing that compliance with legal and regulatory requirements is critical to the development, manufacturing, marketing, and commercialization of medical devices, Mr. Marin combines his engineering and legal expertise to
guide LOK North America’s clients through the growing number of laws
and regulations governing this industry.
His recent contractual experience includes drafting and negotiating intellectual property licenses, collaboration agreements, manufacturing agreements, distribution agreements, research agreements, and quality contracts; and
His recent regulatory experience includes the licensing in Canada and the United States of innovative medical devices such as mobile medical applications using artificial intelligence, closed-loop oxygen therapy devices, dental and orthopedic implants, stereotaxic orthopedic devices, isolation chambers with antimicrobial components, ventilators, electrophotonic particle detectors, multi-frequency impedance meters, and drug pumps with radiopharmaceutical components.
- Standardization and Certification
- Technology Transfer Strategies
- Cybersecurity
- Commercial Law and Contracts
- Strategic Partnerships and Agreements (Licensing)
- Regulatory Law – Medical Devices and Cosmetic Products
- Her recent experience includes drafting and negotiating intellectual property licenses, collaboration agreements, manufacturing contracts, distribution agreements, and research contracts, particularly for high-tech companies. In regulatory matters, she provides support in the development, approval, and post-market surveillance of medical devices.