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.
Led by a former FDA Regulator, TulipLab's veteran regulatory experts provide crucial insights into regulatory operations, leading to the most effective pathway from product to market. Backed by a vast network of scientific, legal and regulatory professionals, you’ll receive dedicated support throughout each step of the process.GET A QUOTE