Regulatory Management

For R&D leaders, product safety teams, and regulatory teams. See ingredient hazards while the formula can still change, load SDS composition from the experiment, and review each change before the SDS goes out.

For regulatory and compliance teams in paint, coatings, and specialty chemicals. See how Uncountable Regulatory screens each recipe by market as it is built, shows the rule and source behind every result, and traces a change across the portfolio.

For regulatory affairs, product stewardship, R&D, quality, and IT teams writing a regulatory software RFP or URS. Get requirements, supplier demo scenarios, and common mistakes for substance rollup, list screening, SDSs, labels, and change impact.

Learn how to translate EU Battery Regulation obligations into battery passport data requirements. Connect product identity, supplier evidence, production records, declarations, and lifecycle information to build a traceable evidence chain.

For cosmetics and personal care R&D leaders. Learn how to connect formulation, testing, variants, claims and compliance data to reduce fragmentation, reuse knowledge, manage product complexity and make faster product decisions.

A white paper specifying the formulation record behind an EU Cosmetic Product Safety Report and a MoCRA substantiation file: composition, impurities, fragrance, and exposure data, field by field, plus five open US regulatory questions.

How Uncountable checks formulations against regulations while they are being formulated, with a status and the regulation behind it for each ingredient, and regulations maintained from official sources.

How food and beverage R&D teams calculate nutrition for every formula and generate allergen statements, ingredient statements and Nutrition Facts labels from the same ingredient data.

How R&D teams keep the safety data sheet linked to the recipe, with all 16 GHS sections as structured fields, composition loaded from the recipe, a review workflow and PDF export.

See how Uncountable puts cosmetics formulation, stability, sensory, and claims data on one searchable record: ingredients screened against regulatory limits live, substitutions propagated automatically, and every claim linked to the data behind it.

Ingredient regulations checked as the formula is built. Uncountable maintains the regulations database, kept up to date from official sources.

A mixture is classified from test data, then bridging, then a calculation from its ingredients. Here's how the acute toxicity formula and skin corrosion limits work, and three data choices that change the result...

An SDS goes out of date when the classification behind it changes, even if the formula doesn't. With new EU CLP hazard classes landing for substances on 1 November 2026, here's how to find the SDSs a reclassification touches...

PDRN is in launches from Primark to Dior, but the materials behind the name come from very different sources. Here's what to record about a supplier grade before you compare test results or sign off a claim.

FDA’s salt substitutes rule gives food manufacturers more room to reduce sodium. Explore what changes for standardized foods, which formulation trials to prioritize, and how connected R&D data supports testing, labeling, and product launch decisions.

The EU’s PFHxA restriction now applies to cosmetics and food-contact paper and board. Learn which concentration limits apply and what records labs should keep, including supplier evidence, test results, formulation versions and batch traceability.

A bill of materials describes components; a bill of substances describes chemical composition. Learn how these views connect with formulas to support product impact assessments, cost calculations, and compliance reviews.

A lab that ships a hazardous chemical counts as a manufacturer or distributor, so every customer sample needs an SDS. Here's why the SDS is usually the slowest step before a sample ships, and how to check your own process...

Uncountable’s Regulatory Management checks recipe ingredients against market-specific requirements as formulations are built, giving teams pass/fail visibility, cited evidence, and early warnings before noncompliant recipes move downstream.

REACH entry 74 changed how polyurethane adhesives and sealants can be sold in the EU. Compare training support, low-monomer prepolymers and silane-modified polymers, and find every product the decision touches...