Food supplement formulation, safety assessment, and regulatory guidance

Supporting your food and nutraceutical products from safety assessment to market authorization.

Ensuring safety and compliance for
innovative food ingredients

Bringing food and nutraceutical products to market requires a firm guarantee of safety for the end consumer. We support industry players at every stage of ingredient and finished product development, whether for human or animal consumption. From scientific safety validation to the preparation of comprehensive regulatory dossiers and applications for innovative ingredients, our expertise helps you streamline and secure your processes. Our multidisciplinary team of toxicologists, chemists, ecotoxicologists, and in silico analysis specialists combines complementary skills to turn your innovations into compliant, reliable products ready to succeed in the market.

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Key regulatory services for

food and nutraceutical products

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Key Services

New products authorisation

Comprehensive support for Novel Foods, NDI, and GRAS dossiers.
Guidance on the authorization of GMO products and food/feed additives.
Preparation and submission of food and feed authorization applications (EU, USA, UK).
Management of communications and follow-up with regulatory authorities.

Comprehensive safety dossier

Preparation of justification dossiers (dose exceedance, absence of labeling, etc.).
Safety evaluation of ingredients, substances, additives, and finished products.
Expert support on safety topics: endocrine disruption, NAMs, in silico analysis, etc.
Support in establishing safety evaluation strategies for raw materials and finished products.

Risk Assessment

Risk analysis via dietary exposure (contaminants, active substances, bioactive compounds, etc.).
Risk assessment for target populations and species.

Formulation Support

Assistance in formulating finished products.
Safety evaluation of candidate ingredients from the early stages of formulation.
Preparation of safety reports for selected ingredients.

Event, Novel Food training

Novel Food & Toxicological assessment:
Selecting, understanding and interpreting key studies

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Looking for guidance on food supplements?

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Innovative food and feed products must obtain regulatory approval before commercialization, which requires demonstrating their high-quality and safety. This involves developing a robust safety assessment strategy to identify and address all potential risks associated with the consumption of these innovations for the relevant populations or species. Our team of experts supports companies throughout the entire process, from defining the toxicological assessment strategy and preparing dossiers to submission and ongoing communication with authorities, ensuring that innovative products reach the market efficiently and safely.

Bringing food and nutraceutical products to market requires ensuring their safety for consumers. Safety dossiers are therefore essential to demonstrate the safety of ingredients, substances, additives, and/or finished nutraceutical products. These dossiers rely on toxicological data or in silico analyses and provide scientific justification when required by regulations (for example, in cases of dose exceedance or absence of labeling). We prepare comprehensive safety dossiers tailored to regulatory requirements to support the successful and compliant introduction of your products to the market.

Safety evaluation should start as early as possible in the product development process. Early assessments help identify potential safety concerns, guide formulation choices, and ensure alignment with regulatory requirements, saving both time and resources when moving toward market approval. Our team can support you throughout this process to secure a smooth and compliant product development pathway.

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