Our team starts all projects with an in-depth review of your product’s complete formula to determine the product classification. There are 3 classes of submission under the NHP regulations, each with its own ingredient requirements – Class I, Class II, and Class III. Class I and II applications rely on pre-cleared monograph evidence for efficacy and safety. Class III applications can require a full review of safety, efficacy and quality data that supports the ingredients and claims listed on the application. The final step once classification is finalized is to file the complete product application, answer any questions that come up through the assessment process, and wait for Health Canada approval. Once approval is received our work is not complete – we are available to assist with compliant labeling, and any product changes that may occur or post-license information request notices.