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Dose Conversion Made Easy for Researchers

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  • Dose justification in NDI-N or GRAS submissions

The methodology is directly based on Guidance for Industry: Estimating the Maximum Safe Starting Dose in Initial Clinical Trials for Therapeutics in Adult Healthy Volunteers. Center for Drug Evaluation and Research (CDER), Food and Drug Administration, the U.S. Department of Health and Human Services, July 2005

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Our tool is freely available to the research community. No sign-up required. Whether you’re planning your next animal study or finalizing a GRAS dossier, this tool helps you make your case with clarity and compliance.

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Disclaimer: The Dose Conversion Tool is intended solely for use by researchers, regulatory affairs professionals, and product developers. It must not be used by consumers to determine personal dosing or to assume safety of any ingredient or product. The Dose Conversion tool does not account for required safety factors, target population considerations, intended use, or regulatory toxicology standards. For any clinical, therapeutic, or consumer use, appropriate safety assessment, expert review, and regulatory compliance are essential.

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