Headquartered in the greater Montreal area, LOK North America caters to national and international clients seeking comprehensive regulatory compliance and quality assurance services for their medical devices.

Our expertise spans regulatory affairs, design control development, quality management, risk identification and management, software verification and validation, and market approval. Our team consists of dynamic experts with diverse backgrounds, bringing a wealth of legal and technical expertise across multiple sectors.

With a deep understanding of quality management requirements, we specialize in crafting tailored solutions for companies participating in the One Audit Program for Medical Devices (OAPM/MDSAP).

Contact us to discuss how we LOK North America can help expedite your medical devices entry to the Canadian market while maintaining the highest standards of compliance.