The Food Additives platform digitizes the Codex Alimentarius General Standard for Food Additives (CXS 192-1995). This covers 306 food additives (ingredients) across 266 food categories, with over 5,100 permission rules including usage limits and regulatory conditions.
How current is the data?
The platform reflects the latest published version of CXS 192-1995. Data is refreshed when Codex publishes updates (typically annually). Your dashboard will always show the most recent data available.
Does the platform cover regulations beyond Codex?
Currently, the Food Additives platform focuses on the Codex Alimentarius international standard. Support for additional jurisdictions (EU, FDA, FSSAI) is on our roadmap.
Can I use the platform for regulatory compliance?
The Food Additives platform is an intelligence and planning tool. It helps you understand regulatory permissions quickly, but it does not replace formal regulatory review. Always verify with your regulatory team or consultant before making compliance decisions.
When a usage limit shows “Open dose (GMP)”, it means there is no fixed maximum level. The ingredient should be used at the minimum quantity needed to achieve its intended effect, consistent with Good Manufacturing Practice.
What do the difficulty ratings mean?
Difficulty ratings (Premium/Enterprise only) indicate how complex a regulatory permission is to interpret:
How is the Commercial Opportunity Score calculated?
The score (0-100) is a weighted composite of five factors: regulatory difficulty (30%), expert review rate (25%), category reach (20%), condition burden (15%), and standards coverage (10%). Higher scores indicate categories where regulatory complexity creates competitive barriers.
What are 'conditions' on a permission rule?
Conditions are regulatory notes attached to specific permissions. They may restrict scope (“only in surface treatment”), add exceptions (“except for infant food”), or define specific use cases. A single rule can have multiple conditions.