Trusted Guidance. Regulatory Expertise. Proven Results.

We deliver expert regulatory support for Natural Health Products and foods, including Health Canada licence applications, labelling, claims substantiation, and GMP compliance. We also assist with U.S. FDA dietary supplement regulations to support seamless cross-border market entry.

We provide comprehensive regulatory consulting for cosmetics, covering Health Canada ingredient assessments, labelling requirements, notifications, and safety documentation. Our services extend to U.S. FDA cosmetic compliance, helping you launch products efficiently on both sides of the border.

We offer specialized support for medical devices (Class I–III), including Health Canada licensing, quality system implementation, and post-market obligations. We also guide clients through U.S. FDA 510(k) and other regulatory pathways for efficient North American market access.

We build and maintain robust Quality Management Systems (QMS) and facility compliance programs, including GMP audits, SOP development, and site licensing. Our practical approach covers both Health Canada and U.S. FDA requirements, delivering audit-ready solutions without big-firm costs.