Market Access Intelligence for Industry.
One substance becomes a chain of duties: registration, classification, communication. Know what you can place, where, and keep every SDS, label and notification current as the lists move.
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 list moves, and the obligation lands on everything that contains it.
substances of very high concern sit on the REACH candidate list, each able to trigger notification and communication duties down your chain.ECHA SVHC candidate list
substances are registered under REACH, so a single restriction or reclassification ripples across countless downstream products.ECHA registered substances
a universal restriction under assessment could sweep thousands of substances and articles into scope in one move.ECHA restriction proposal
packaging, recycled-content and extended-producer-responsibility rules now add market-by-market duties on top of the chemistry.EU Packaging & Packaging Waste Regulation
You inherit the duty for what's inside, even when you didn't formulate it.
A substance is added to the REACH candidate list, and anywhere it sits above threshold, in a mixture, in a component, in an article, you inherit notification and communication duties overnight. A supplier reclassifies a raw material, and your CLP labels and safety data sheets cascade across every product that uses it. Extended-producer-responsibility rules add obligations by geography; a universal PFAS restriction hangs over whole product families. The work is knowing at once which products just took on a duty, and by when.
One candidate-list addition can trigger notification, communication and, eventually, authorisation duties across every product and article containing it, often before you know it's there.
A single raw-material reclassification leads to label changes and safety-data-sheet revisions across every downstream mixture. Each revision has to be fast and traceable.
Broad restriction proposals can sweep whole substance families into scope. Knowing which of your products sit in the likely net, and when, is the planning question.
Extended producer responsibility, packaging and take-back rules add market-by-market duties that decide whether you can place a product at all.
You owe communication, and sometimes notification, for substances inside components you buy. Your compliance depends on your suppliers' declarations being right.
Once a substance hits the authorisation list, a sunset date starts a countdown to substitution, whether or not an alternative is ready.
The Prodeen platform catches each candidate-list addition, reclassification and restriction proposal and matches it to your substances, mixtures and articles. Your team gets a next step, files notifications on time and plans substitutions early.
See the signal in actionOne substance went onto the candidate list on a Thursday. By Friday the questions were: which of our mixtures contain it, which articles, above which threshold, in which markets, and who do we have to notify, and by when? Done by hand, that takes a fortnight of cross-referencing. With Prodeen, the team gets a validated event with the duties already listed.
The SDS cascade starts the moment a supplier reclassifies a raw material.Everything that decides if a product can be placed, in one view.
One candidate-list addition reaches Regulatory, Product Stewardship, Quality, R&D and Procurement, each with its next step. Prodeen tracks the five domains below and turns each signal into an action.
One loop, from a list addition to a filed notification.
| EU | UK | US | CN | |
|---|---|---|---|---|
| SVHC presence | ||||
| PFAS exposure | ||||
| CLP classification | ||||
| Packaging / EPR |
Six product stewardship jobs, from a new market to a sample report.
Check the substance against the rulebook
Before you enter, know the registration you'll owe, the restrictions in force, and the packaging and EPR duties that apply.
See the use case →Launch with the SDS right first time
Validate classification, labelling and restricted-substance status across every launch market before you place the product.
See the use case →Keep every SDS & notification current
Prodeen routes every SVHC addition, reclassification and restriction to the mixtures and articles it touches, as it happens.
See the use case →Evidence every duty was met
Keep a signed record of notifications, classifications and communications for each market, ready for any inspection.
See the use case →Swap raw lists for routed duties
Stop cross-referencing candidate and restriction lists by hand. Get changes routed to your substances, with the duty drafted.
See the use case →Bring us one substance
Send us one substance, one product and one market. We will send back a sample report on the duties it carries.
Test us →