FDA mandates all foods – those that have been genetically modified – as
well as those manufactured through new processes, with no history of safe use, to be considered as novel foods.
All these need country-specific re-assessments.
But is your product a novel food? What is the process for completing the required federal assessments?
TulipLab’s expert regulatory team will guide your business through both these stages. Our expert team conducts a
technical review that studies safety requirements. Post analysis, we secure the required evidence for completing
a re-assessment.
Finally, our expert regulatory toxicologists complete your application and ensure that requirements are met
till the process is completed.
