Market Access Intelligence for Ingredients.
Your customers sell into many markets, so your ingredient has to comply in all of them. Every spec and every COA has to hold as the rules change.
See how it works ↓Market Access Intelligence for beverages: one living view of the taxes, thresholds, sweetener rules, caffeine limits, label laws and claim trends that decide whether a drink reaches the shelf, and stays on it.
What is Market Access Intelligence? →A rule change hits the ingredient first, then every customer recipe that uses it.
food and feed safety notifications are raised in the EU each year. Raw materials and ingredients are among the products most often cited.EU RASFF annual report
legacy food additives are in the EFSA re-evaluation programme. One outcome can reach every customer recipe that uses the additive.EFSA additive re-evaluation programme
pesticides have maximum residue limits that your incoming COAs must clear, and those limits keep tightening.EU MRL database
hazards behind EU alerts are mycotoxins, pesticide residues and pathogens. All three are raw-material problems that show up on a COA.EU RASFF hazard categories
You inherit the compliance requirements of every market your customers sell into.
A CPG brand worries about its own markets. You inherit every one of them. One colour, one enzyme, one protein can sit inside hundreds of recipes shipping into dozens of jurisdictions, each with its own permitted list, purity criteria and labelling knock-on. When EFSA re-opens an additive, when an MRL drops, when a contaminant limit tightens, the question is which grades, lots, customers and markets it affects, and how fast you can tell them. Today that answer can take a regulatory team a week. With Prodeen, the team validates a drafted answer within hours.
A re-evaluation or MRL change hits your ingredient before it hits any finished product. Miss it, and you ship non-compliance downstream to everyone who trusts your spec.
Every prospect and audit brings a stack of "is it compliant in our markets, does it meet our claims" questions. Your team answers them by hand, and each answer holds only until the next rule change.
Take cadmium in cocoa, heavy metals in minerals or mycotoxins in botanicals. A COA number only means something against each destination market's limit.
GRAS conclusions, novel-food authorisations and purity specs make up the evidence file that lets an ingredient be sold. When the underlying rule moves, the dossier has to move with it.
The same ingredient can be permitted in food but not in supplements, allowed in the EU but pending in the US, cleared for adults but limited for infant categories. So one ingredient can get a different answer in each market and use.
When a downstream additive is restricted, your customers come to you for the replacement, fast. A supplier with a compliant alternative ready keeps the customer's business.
The Prodeen platform catches each re-evaluation, MRL revision and COA result and matches it to your grades and customers' markets. Your team gets a next step it can act on, answers questionnaires in hours and keeps dossiers current.
See the signal in actionThe COA said cadmium 0.68 mg/kg. That is within most markets' limits but over the EU limit for cocoa powder sold to consumers. The same lot gets two different verdicts. What matters is knowing at once which of your 200 customers now has a problem.
Then you can call those customers before they find the problem themselves.Everything that decides if your ingredient can ship, in one view.
One re-evaluation reaches Regulatory, Quality, R&D, Procurement and Commercial, each with its next step. Prodeen tracks the five domains below and turns each signal into an action.
One loop, from an EFSA opinion to a customer notification.
| EU | US | BR | JP | |
|---|---|---|---|---|
| Additive re-evaluations | ||||
| Pesticide MRLs | ||||
| Heavy metals | ||||
| Mycotoxins |
Six ingredient jobs, from qualifying a grade to a sample impact report.
Qualify a grade for a new region
Confirm permitted use, purity criteria and labelling knock-ons before you promise a customer you can supply there.
See the use case → Launching a productBring a new ingredient to market
Map the approval route (GRAS, novel food or pre-market notification) and build one dossier that works for every destination.
Managing a live portfolioKeep every spec and dossier current
Prodeen checks every re-evaluation, MRL change and COA against your grades and your customers' markets as it happens.
Preparing for an auditAnswer the customer questionnaire in hours
Keep a signed, current evidence file for each grade, so audits and RFIs no longer take your senior team's week.
Replacing a legacy subscriptionTrade a raw feed for routed intelligence
Stop scanning a database that doesn't know your grades. Get events pre-filtered to your specs and your customers.
Not sure yet?Bring us one spec
Send us one ingredient, one COA and one customer market. We will send back a sample impact report built on your data.
Test us →Ingredient teams get a validated impact read within hours of a rule change.
From an EFSA re-evaluation or MRL change to a validated impact read your team can act on, with every source named.
Of incoming signals filtered out as noise before they ever reach your team.Illustrative, based on a typical ingredient portfolio.
Your team answers customer regulatory questionnaires from one current evidence file.
Built by the team behind Selerant and DigiComply. This is our third time in your world.