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Answer a few guided questions. Complivare searches live Health Canada registries — 4.4M+ records — to determine your regulatory pathway, device class, and licensing requirements.
Have a product description, label text, or instructions? Add them here to reduce typing. No documents? Continue directly with the form below.
Text files up to 250 KB, or Word, PDF and PNG/JPEG images up to 10 MB. Extraction runs locally in your browser using first-party hosted document libraries. OCR language data may be downloaded once; document contents are not uploaded automatically. Review all extracted information.
Your description suggests a possible drug pathway. These details help assess the product; the final category depends on its ingredients, claims and intended use.
Not sure about a detail? You can continue. Complivare may request clarification where it affects the regulatory pathway.
Look up any NPN in the live Licensed Natural Health Products Database and get product details, licence status, and monograph alignment.
Select your product category and answer four questions to get a scored compliance assessment with specific gaps and next steps.
Enter any product claim and Complivare checks it against Health Canada rules — for NHPs, Medical Devices, Drugs, and Cosmetics — and suggests a compliant rewrite if needed.
Search any ingredient to get its regulatory status in Canada, applicable HC monograph, dosage limits, restrictions, and approved products that use it.
Before importing or selling a medical device in Canada, verify it is registered in Health Canada's Medical Devices Active Licence Listing (MDALL). Search by device name, licence number, or company — anyone selling an unlicensed device risks regulatory action.
Before marketing a drug product in Canada, confirm it has an active Drug Identification Number (DIN) issued by Health Canada. A DIN means the product has passed Health Canada's review of its formulation, labelling, and instructions. No DIN means no legal sale.
Tool uses are counted only when a result is successfully returned.
Used to personalise your regulatory experience.
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