Stay compliant with FDA drug establishment and listing renewal requirements before December 31, 2025. Learn key steps and how to file correctly.
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Learn how CETA allows EU exporters to sell food supplements in Canada tariff free and what regulatory steps are required for compliance.
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Learn the key differences between importing human food and animal food into Canada, including CFIA and Health Canada requirements.
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Learn how an expert panel supports GRAS determinations by ensuring scientific credibility, safety, and FDA alignment.
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Learn how to get GRAS status for an enzyme and meet FDA safety requirements through proper evaluation, expert review, and documentation.
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Learn how to prepare and submit an EFSA novel food application and gain market access in the EU.
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Learn how clinical studies support EFSA novel food applications, ensuring your product’s safety, efficacy, and market approval.
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FDA confirms NMN is lawful in dietary supplements after industry pressure. Learn what this means for your business and compliance strategy.
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Learn how to prepare Instructions for Use for FDA submission for medical devices. Stay compliant with FDA requirements and international standards.
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FDA proposes ending the self-affirmed GRAS pathway. Learn what this means for your business and how to stay compliant.
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Discover the truth about SR&ED eligibility myths and learn what actually qualifies for credits and refunds under Canada’s SR&ED program.
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What is SR&ED and how does it work in Canada? Learn about eligibility, benefits, and how to maximize your SR&ED tax credit with expert guidance.
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