Learn how to register a private label medical device with Health Canada. Follow this step-by-step guide to ensure regulatory compliance.
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FDA’s new EDT tool helps screen chemicals in food for toxicity. Learn how it supports safer food and faster evaluations.
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Learn how a new bill may eliminate self-affirmed GRAS and what it means for food ingredient compliance. Stay ahead with expert support.
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FDA approves gardenia (genipin) blue color additive while encouraging a faster phase-out of FD&C Red No. 3. Learn how this impacts your products.
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Learn how the SAFE Sunscreen Standards Act could impact sunscreen compliance and FDA approvals.
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Learn how to avoid site license renewal refusals or suspensions and meet Health Canada compliance expectations.
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Learn how CFIA’s feed regulatory modernization impacts your compliance. Stay ahead with key changes and expert guidance.
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Introduction Sodium reduction in processed foods is no longer optional. It is a critical step for industry players to safeguard consumer health and meet Health
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The FDA Food labeling compliance program has just been updated to help food manufacturers and importers meet U.S. labeling requirements more effectively. On June 20, 2025, the U.S. Food and Drug Administration (FDA) announced a revised Compliance Program Manual (CPM) for general food labeling.
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When preparing to launch a medical device in the U.S., one of the first and most important decisions
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If you work in the life sciences industry, you’ve likely heard of GMP, Good Manufacturing Practice. It’s a fundamental part of producing safe, effective, and high-quality products.
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When it comes to audits related to Health Canada requirements, staying compliant is about more than checking off a list. It helps you maintain your
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