Learn how to prepare and submit an EFSA novel food application and gain market access in the EU.
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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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Discover 10 best practices to achieve GRAS status while staying FDA compliant. Follow expert tips for smooth ingredient compliance.
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Explore the 7 sections of a GRAS dossier and learn how they ensure ingredient compliance, safety, and FDA acceptance.
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Learn how the FDA’s new cosmetic adverse event reporting dashboard works and what it means for your compliance strategy.
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Learn what’s new in Health Canada’s GMP guide for NHPs. Discover updates, transition timelines, and compliance steps for your business.
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