Chemply
Chemply is a modern platform for authoring, approving, and maintaining Safety Data Sheets. Built for the people responsible for getting hazard communication right — and keeping it right, document after document.
An SDS is a living document. Substances change, formulations change, and regulations change. Without a system of record, that complexity quickly becomes a compliance liability — and the people responsible carry it.
A reformulation, a new supplier, an updated reference value — and the published SDS no longer matches reality. Without explicit version control, those gaps go unnoticed until an audit surfaces them.
Sign-off threads scattered across email, Slack, and tracked-change Word files leave you without a clean record of who reviewed what — and when. Regulators expect an unambiguous audit trail.
Hazard classifications, CAS lookups, regulatory limits and language translations get reconstructed for every new document. Knowledge that should be reusable becomes copy-paste — and copy-paste mistakes.
Chemply is built around the four things that make SDS work scale: a structured authoring engine, every revision on the record, approvals you can defend, and curated reference data you don't have to maintain.
Build a complete 16-section Safety Data Sheet from a substance, a mixture, or a finished product. Hazard classification follows GHS Rev. 9 conventions and OSHA HazCom 2012 formatting, with editable output at every step.
Every revision of every SDS is preserved with a timestamp, the author, and a structured diff against the prior version. Roll back, compare side-by-side, or pin the version that shipped with a specific batch.
Define reviewers per section, per product, or per organization. Every approval is signed, timestamped, and attributed — producing a continuous, exportable audit trail from draft to published document.
A maintained reference library of substances, hazard classifications, regulatory data and translated phrase banks. Bring your own private catalog or extend ours — both stay versioned and searchable across your workspace.
A predictable pipeline with explicit checkpoints. No spreadsheets, no tracked-change Word files, no scattered approvals.
Pull from the curated catalog or create a new record. Mixtures are built component-by-component, with confidential composition supported.
Generate a structured draft, edit any section, and route through your reviewer chain. Each change is captured against the prior version.
A signed, timestamped approval record locks the published version. Future revisions inherit the audit trail automatically.
Chemply is built for three groups of people who already do this work well. We make their day faster — we don't replace their judgment.
A workspace per client, full version history, and an audit trail your clients can take with them. Consultants are a first-class tier — not an afterthought.
Manage a growing product line with shared catalogs, configurable reviewer chains, and SDS versions you can pin to specific batches and shipments.
Multi-team workspaces, role-based access, single sign-on, and the governance controls your regulatory department already requires.
One predictable monthly rate per tier. Unlimited revisions within your plan. Annual billing available with a 20% discount.
Purchase a single Safety Data Sheet without a subscription — same authoring engine, same version history, same audit trail. Discounts apply automatically when you buy in bundles.
All plans include unlimited revisions and the full audit trail. Have a larger team or special requirements? Get in touch →
A few questions we hear most often from regulatory professionals evaluating the platform.
The authoring engine follows OSHA HazCom 2012 formatting and GHS Rev. 7 conventions for hazard classification. Additional regional standards are on the roadmap; we're transparent about what's supported today versus in development.
No. Chemply is a platform that helps regulatory professionals — independent or in-house — do their work faster and with a cleaner audit trail. Final responsibility for classification and publication always rests with a qualified reviewer.
Every approval action is captured with the reviewer's identity, a timestamp, and a reference to the exact document version they approved. The full chain — draft, edits, reviewer sign-offs, publication — is exportable as a single record.
You do. Your substances, products, formulas, and SDS revisions belong to your organization, are not used to train external models, and can be exported in standard formats at any time.
Every substance and product carries its own version timeline. When a substance is updated, downstream products that reference it surface the change so you can review impact before re-publishing.
Every plan starts with a 14-day free trial. No credit card is required to sign up, and you have full access to authoring, version history, approvals, and the curated catalog during the trial.
Start your 14-day free trial. No credit card required. Cancel anytime.
Or email us directly at [email protected].
Chemply