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 job isn't reading the list. It's knowing, instantly, which products just inherited 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 ripples into label changes and safety-data-sheet revisions across every downstream mixture, fast, and traceably.
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 bought, not made, so 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.
This is exactly what Prodeen is built for: every candidate-list addition, reclassification and restriction proposal caught the moment it moves, matched to your substances, mixtures and articles, delivered as a next step your team can act on, not another signal to triage. Notifications filed on time. SDS cascades that finish. Substitutions planned, not forced.
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? The old way, that's a fortnight of cross-referencing. It has to be a validated event with the duties already listed.
and the SDS cascade starts the moment a supplier reclassifies.Everything that decides if a product can be placed, in one view.
Regulatory, Product Stewardship, Quality, R&D, Procurement: one candidate-list addition reaches everyone, next step attached. Five connected domains. Signals that turn into action, not alerts to triage.
One loop, from a list addition to a filed notification.
| EU | UK | US | CN | |
|---|---|---|---|---|
| SVHC presence | ||||
| PFAS exposure | ||||
| CLP classification | ||||
| Packaging / EPR |
Every substance, every article, every market.
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 → Launching a productLaunch 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 → Managing a live portfolioKeep every SDS & notification current
Every SVHC addition, reclassification and restriction routed to the exact mixtures and articles it touches, continuously.
See the use case → Preparing for an auditEvidence every duty was met
A signed, current trail of notifications, classifications and communications, inspection-ready, per market.
See the use case → Replacing a legacy subscriptionSwap 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 → Not sure yet?Bring us one substance
One substance, one product, one market. We'll send back a sample report on the duties it carries.
Test us →The discipline, applied beyond the shelf.
From an SVHC addition or SDS change to a validated answer your team can action, every source named.
Of incoming signals filtered out as noise before they ever reach your team.Illustrative, based on a typical substance portfolio.
An SVHC addition traced to every affected mixture and article in hours, not a fortnight of cross-referencing.
Built by the team behind Selerant and DigiComply. This is our third time in your world.