Regulatory Consulting

ACC ’s regulatory Consulting team provides comprehensive services for food, dietary supplements, and feed across the entire food supply chain. We help our clients in their regulatory compliance needs in the USA, EU, Australia and New Zealand, Canada, Singapore, and China.

USA Regulatory Compliance Consulting

Our regulatory filing services include self-affirmed Generally Recognized As Safe (GRAS) determinations, submission of GRAS Notices to FDA, Flavor and Extract Manufacturers Association (FEMA) GRAS submissions for flavors and fragrances, Food Additive Petitions (FAP), New Dietary Ingredient Notifications (NDIN), animal food ingredient GRAS submissions, and compliance support for the Foreign Supplier Verification Program (FSVP).

We also provide feasibility assessments, data gap analyses, toxicology and exposure assessments, GRAS expert panel coordination, dossier preparation and compilation, liaison with the FDA and response to information requests, as well as U.S. agent support for foreign suppliers, where applicable.

EU Regulatory Compliance Consulting

Our regulatory filing services include applications for Novel Foods, Food Additives, Food Enzymes, Flavourings, and Feed Additives.

We provide pre-submission support and Notification of Studies (NoS), feasibility assessments, data gap analyses, toxicology and exposure assessments, dossier preparation and compilation, liaison with European Union (EU) authorities and responses to information requests, as well as EU representative services where required.

Regulatory Compliance Consulting in Other Countries

Our regulatory filing services cover Food Standards Australia New Zealand (FSANZ) Novel Foods in Australia and New Zealand, Therapeutic Goods Administration (TGA) Permissible Ingredients in Australia, Novel Foods and Natural Health Products (NHPs) in Canada, Novel Foods in Singapore, as well as New Food Raw Materials and New Food Additives in China.

We also provide local regulatory agent support where required, feasibility assessments, data gap analyses, toxicology and exposure assessments, dossier preparation and compilation, and liaison with authorities, including responses to information requests.

Our advantages

Multilingual Technical Team

An international team of food scientists, quality control and GMP experts, nutritionists, toxicologists, and specialists in various food and feed categories.
Multi -language team based in Shanghai, Malaysia, USA, and Germany.
Extensive due diligence is carried out with our clients’ product development team and quality assurance team. Our specialists work directly with clients on-site to clarify requirements, identify gaps, and provide actionable guidance that streamlines submissions and minimizes rework.

Extensive Expert Resources

We collaborate with senior regulatory experts across the U.S., EU, Australia and New Zealand, Singapore, and Canada, with expertise in botanicals, fermentation and synthetic biology, toxicology, chemistry, and nutritional sciences. Our team of experts has hands-on experience with filings for food, dietary supplements, pharmaceuticals, and feed, and a strong understanding of review priorities and compliance nuances across jurisdictions.

End-to-End Service Capability

ACC provides comprehensive compliance support, ranging from feasibility assessments and dossier preparation to GMP/HACCP implementation, assistance with toxicology studies, systematic literature reviews, and responses to authority inquiries—ensuring projects progress efficiently.

Time and Cost Advantages

Wherever you are in your preparation, ACC provides flexible support. You can share a draft for us to enhance, or let us handle the full preparation and submission process. With faster response times, clear deliverables, and closer collaboration, we offer advantages over overseas providers.

LMS compliance Ltd.