Navigate Global Color Additive Approval with Strategic Regulatory Expertise
Bringing a food color additive to market in the U.S., EU, China, Canada, or Japan requires navigating region-specific regulatory frameworks, each with unique safety standards, petition processes, and labeling rules. In the U.S. and EU, color additives must be pre-approved through formal petitions demonstrating safety for intended use. In other global markets, ingredients must comply with positive lists, maximum use levels, and purity specifications.
Why Choose Intertek for Color Additive Approval?
Intertek Assuris provides trusted regulatory and scientific consulting to help you manage these complexities with confidence and precision. When it comes to strategic consulting for color additive approval, Intertek stands out with unmatched global expertise and proven success. Choosing Intertek means choosing:
- End-to-end petition support for FDA color additive approvals, including exemption pathways
- Clear guidance on additive requirements from the European Commission (EU), CAA (Japan), CFSA (China), and Health Canada
- Expert analysis of labeling, classification, and permissible use levels
- Strategic risk mitigation to reduce regulatory delays and accelerate market entry
- Multisector expertise, from food and dietary supplements to cosmetics and pharmaceuticals
Don’t risk costly delays or rejections. With Intertek, you benefit from science-backed strategies and a deep understanding of evolving global requirements.
Our Comprehensive Regulatory Services
Whether launching a novel color additive or reformulating for a new market, Intertek delivers focused support tailored to your regulatory goals:
- FDA Color Additive Petition Preparation and Submission
- Toxicology Data Development & Gap Assessments
- Exposure Modeling & Dietary Intake Estimation
- Regulatory Intelligence for Global Market Compliance
- Strategic Positioning of Natural and Novel Colorants
From concept to clearance, we help you meet global expectations — efficiently and compliantly.
Related Expertise
Explore complementary services that support your product’s full regulatory lifecycle:
- Food Additive and Ingredient Regulatory Consulting
- GRAS and Novel Food Submissions
- Toxicology and Safety Assessment
- International Market Access Strategy
- Claims Review and Substantiation
Ready to bring your color additive to market?
Let’s make it happen — safely, strategically, and globally.
Request a Consultation or speak with an expert today.
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