TotalSDS by Enhesa pairs a regulatory team with SDS authoring software so classification, labeling, and hazard communication stay correct as OSHA HazCom, GHS, and regional rules evolve — no in-house toxicologist required.
Compliance expertise, without hiring a chemist.
Do you need regulatory consulting, or just better software?
Regulations have changed since your SDS library was last reviewed, and you need a gap analysis before something slips.
A new chemical or reformulated product needs classification and an SDS that aligns with your compliance framework.
You need expert validation or updates to your documentation before a third-party review or regulator inspection.
Distributing internationally means SDSs need to reflect local language and regulatory requirements, not just a translation.
Certain criteria — like acute or aquatic toxicity — require expert judgment when test data is limited or absent.
Seven ways our regulatory team keeps you compliant
SDS Authoring & Updates
Drafting new Safety Data Sheets to global regulations, and revising existing SDSs to reflect new data, regulatory changes, or updated classification and labeling.
Regulatory Compliance
Gap analysis that identifies and addresses compliance gaps in your existing SDS documentation before they become audit findings.
Transportation Classification
Determining the appropriate DOT transport classification for chemicals and products based on current regulatory criteria.
Hazard Communication
Training sessions on understanding and using SDSs and labels, plus consultation on best practices for safe chemical handling.
Consultation & Support
Technical support for specific chemical safety and compliance questions, plus guidance on regulatory submissions like Poison Center Notifications.
Confidential Business Info
Assisting with ingredient masking to conceal proprietary formulation details to the maximum extent while staying compliant.
Classification & Labeling
Product classification assessment — including acute and aquatic toxicity calls outside the standard wizard — plus compliant label development.
From compliance gap to resolved documentation, in four steps
Share your challenge
Tell us what’s prompting the review — new product, audit prep, market expansion, or a documentation gap you’ve spotted.
Regulatory team assesses
Our team reviews the relevant products, ingredients, and jurisdictions to identify what needs to change.
Documentation is resolved
SDSs, labels, and classifications are authored or revised directly, backed by our software and CAS library.
You stay current
As regulations change going forward, updates flow through your SDS library instead of landing on your desk unannounced.
Built for teams that can't afford a compliance gap
EHS & Regulatory Affairs Managers
Need a trusted second set of eyes on classification calls and an audit-ready compliance history.
Product Stewardship & Formulation Teams
Launching new or reformulated products and need classification confirmed before commercial release.
Multi-Site Manufacturers & Distributors
Managing compliance obligations across facilities, business units, or private-label product lines.
Companies Expanding Internationally
Entering new markets and needing SDSs and labels that reflect local language and regulatory requirements.
Quality Assurance & Compliance Managers
Preparing for internal audits or third-party inspections and need documentation validated ahead of time.
Lean Teams Without In-House Chemists
Handling hazardous materials without a dedicated toxicologist or regulatory specialist on staff.
- Cargill
- McCormick
- Patterson Companies
- Aon
- + more*
What compliance and regulatory leaders say
SDS regulatory & compliance
consulting, answered
When does a company need SDS regulatory consulting?
Regulatory consulting typically becomes valuable during new product development, before internal or external audits, when expanding into new markets, or whenever an organization is unsure if its existing SDSs reflect current OSHA HazCom, GHS, or regional regulations.
Do I need in-house chemical expertise to stay compliant?
No. TotalSDS’s regulatory team and authoring software are built so organizations without a dedicated toxicologist or regulatory specialist can still produce and maintain compliant SDSs, with expert support available for edge cases like acute or aquatic toxicity classification.
What is a gap analysis, and do I need one?
A gap analysis reviews existing SDS documentation against current regulatory requirements to identify what’s missing or outdated. It’s typically recommended before an audit, after a significant regulatory change, or when a company hasn’t reviewed its SDS library in some time.
Can TotalSDS help with international or multi-language SDSs?
Yes. When distributing into new markets, TotalSDS’s regulatory team helps ensure SDSs and labels reflect both the target language and the local regulatory framework, rather than relying on direct translation alone.
How does TotalSDS handle confidential business information (CBI)?
TotalSDS’s regulatory team assists with ingredient masking, helping organizations conceal proprietary formulation details to the maximum extent permitted while still meeting hazard communication requirements.
Pair regulatory consulting with our software
SDS Author
Guided classification and authoring software our regulatory team uses to resolve gaps directly.
SDS Manager
A centralized library so compliant SDSs stay accessible across every site once they’re resolved.
SDS Translation
Multi-language SDS support for organizations expanding into new international markets.
