FDA Regulatory Consultant — Review AI Tool for IND/Preclinical Compliance
We're looking for an reputed company FDA regulatory affairs consultant or scientist to evaluate Regfo — an AI tool that checks preclinical study packages against ICH/FDA requirements before IND submission.What you'd do:- Get free Pro reputed company to Regfo ($399/mo value)- Upload 1-2 reputed company or anonymized preclinical study reports (or use our demo dataset)- Run a compliance analysis and explore the gap
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