You already receive regulatory updates. The challenge is identifying your exposure. Valenc's monitoring agents track OSHA, EPA, REACH, CLP, and other regulatory lists in every region where you operate. Each change is compared to the substances and mixtures in your library, and affected SDSs are flagged for review. You receive a bulletin detailing the changes and which of your products are impacted.
Compliance teams already receive newsletters, agency notices, and vendor alerts. The real work begins after the announcement: determining whether the change affects any substance, mixture, classification, or SDS in your portfolio, and identifying which ones. Most teams rely on manual spreadsheet searches and reviewing PDFs. Valenc streamlines this process by using existing product data to provide immediate answers.
Valenc imports new regulatory information for all supported jurisdictions and lists.
Each change is evaluated against the substances, materials, and mixtures in your account. If a substance is reclassified in one jurisdiction, every product containing it is identified.
Each affected product appears in the review queue, showing the change, the impacted component, and the required decision.
Legacy platforms deliver regulatory content on a set release cycle, which can delay updates by months. Valenc's rules engine updates as soon as regulators publish changes, and monitoring agents flag affected SDSs immediately. Regulations are updated in real time, and your SDSs should be too.
What changed? Which product or component is affected? What decision is required? Every alert answers these questions before you open a document. Reviewers can view the product composition, current classification, related SDS variants, and the regulatory change in one place.
A change in substance classification can alter mixture classification, affecting Section 2, label elements, and all language variants. Since monitoring, classification, and authoring use a single product record, Valenc tracks the change throughout the process: the product returns to classification review, affected SDS sections are identified for re-authoring, and updates are routed for approval.
Not every change should trigger an automatic product decision, and Valenc ensures none do. When product data and rules support a clear outcome, the rules engine applies it and sends the result for review. If a change creates ambiguity, such as a concentration range crossing a new cut-off, the exception is flagged for manual resolution. No published SDS is updated without approval.
A change in one jurisdiction does not require action for every market version of a product. Valenc attaches the relevant jurisdiction to each alert, so a CLP ATP flags EU variants and an HCS change flags US ones. Regional changes prompt regional reviews.
Regulatory monitoring software continuously tracks changes in chemical regulations and automatically maps them to the substances, mixtures, and safety data sheets (SDSs) in your portfolio that may be impacted.
Valenc monitors OSHA, EPA, REACH, CLP, and a comprehensive set of regulatory and substance lists across all supported jurisdictions, covering more than 80 jurisdictions as of version 1.0.
Valenc automatically matches each regulatory change against the substances and mixtures in your account, flagging every product that contains an affected component for review.
No. Affected products are always flagged for review. When the rules engine can resolve an outcome, the result is sent for review; if not, the exception is surfaced for a decision before any change is made.
Yes. Each alert provides a clear explanation of the regulatory change, the specific component affected, and the relevant jurisdiction, giving you full transparency into why action is needed.
Rule changes are incorporated as fast as regulators publish them, so your product data and SDSs reflect the current requirements.
See how Valenc links regulatory changes to affected products and enables reviewers to move from update to decision on a single screen.