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EXPERTISE · SAFETY DATA SHEETS

Safety Data Sheets

Authoring, assessing and maintaining safety data sheets to UK and EU REACH and CLP requirements.

The document that carries your classification into the real world.

A safety data sheet has to be provided for any substance or mixture classified as hazardous under CLP, for persistent, bioaccumulative and toxic substances, and for any Candidate List substance present above 0.1% by weight in a mixture — and on request in some other cases. Its format and content are set out in REACH Annex II, as amended by Regulation (EU) 2020/878, structured into 16 mandatory sections in a fixed order.
An SDS is only as reliable as the classification, exposure and use information that feeds into it. Get any of that wrong upstream, and the SDS carries the error straight through to everyone downstream who relies on it.
SDS authoring to current REACH Annex II and CLP requirements
Assessment and audit of existing SDS portfolios
Classification and exposure scenario integration
GB and EU SDS alignment and review
THE 16-SECTION FORMAT

A fixed structure, in a fixed order.

Every SDS follows the same 16-section structure set out in Annex II, so that anyone reading one, anywhere in the supply chain, knows exactly where to find a given piece of information. Sections cannot be left blank without a stated reason, and each has its own defined sub-headings.

1. Identification
2. Hazard(s) identification
3. Composition / information on ingredients
4. First-aid measures
5. Fire-fighting measures
6. Accidental release measures
7. Handling and storage
8. Exposure controls / personal protection
9. Physical and chemical properties
10. Stability and reactivity
11. Toxicological information
12. Ecological information
13. Disposal considerations
14. Transport information
15. Regulatory information
16. Other information
EXTENDED SAFETY DATA SHEETS (eSDS)

When an SDS needs exposure scenarios attached.

An extended SDS (eSDS) is a standard 16-section SDS with one or more exposure scenarios annexed, as provided for under Article 31(7). It applies where a substance has been registered above 10 tonnes a year and required a Chemical Safety Report — the annexed scenarios set out the operating conditions and risk management measures behind each identified use.

Receiving an eSDS carries its own duty: under Article 37(5), a downstream user has to check whether their actual use is covered by the scenarios annexed. If it is not, the options are to adopt the conditions described, raise the use with the supplier so it can be added to a future version, or prepare a downstream user Chemical Safety Report of their own.

Identifying which substances in a portfolio require an eSDS
Building exposure scenarios that reflect real operating conditions
Checking whether your own use is covered by scenarios you receive
Preparing a downstream user CSR where a use falls outside them
AUTHORING TO REACH & CLP

The document is only as good as the data behind it.

Authoring an SDS is not really a writing exercise; it is an exercise in pulling together data that has to be correct before the document is even started. The classification in Section 2 has to match the current CLP classification, the composition in Section 3 has to reflect the actual formulation, and the exposure controls and toxicological information have to be consistent with any Chemical Safety Report and exposure scenarios that sit behind the substance.

Where a substance carries a Chemical Safety Report, an extended SDS (eSDS) with exposure scenarios annexed is required, setting out the conditions of use the risk assessment is based on. Getting an eSDS wrong is one of the more common gaps we find, because the annexed exposure scenarios have to genuinely reflect how the product is used downstream, not a generic template.

Classification, labelling and composition data drawn through accurately from CLP
Exposure scenario integration for substances requiring an extended SDS (eSDS)
Consistent hazard information across the SDS, the label and any transport documentation
Language and format requirements met for the market the SDS is supplied into
SDS AUTHORING SERVICE

We don’t just review safety data sheets — we write them.

If you need safety data sheets creating from scratch — for a new product, a reformulation, or a range that has never had a properly authored SDS — we can produce them for you directly: classification, the full 16-section document, and an extended SDS with exposure scenarios where one is required.

ASSESSING EXISTING SDS

A significant share of SDS in circulation would not pass a proper check.

A large proportion of SDS in circulation are not fully compliant. An EU-wide enforcement project run by ECHA’s Forum, checking over 2,500 safety data sheets across 28 EU and EEA countries, found roughly one in three to be non-compliant — and that was among SDS already in active use, not a sample of obviously poor documents.

Assessing an existing SDS portfolio means checking it section by section against the current legal requirements and against the product it actually describes, not just confirming that all 16 headings are present. The most common gaps we find sit in the classification, the exposure controls, and consistency between the SDS and the product label.

Section-by-section compliance review against current REACH and CLP requirements
Consistency checks between the SDS, the label and the classification on record
Prioritised findings, so the highest-risk SDS in a portfolio get fixed first
Portfolio-wide audits ahead of a market entry, acquisition or customer review
WHEN AN SDS MUST BE UPDATED

An SDS is not filed once and left alone.

Under Article 31(9), specific triggers create a legal duty to update an SDS without delay, and to supply the revised version free of charge to anyone who has received the substance or mixture in the preceding 12 months. Many organisations also review SDS on a rolling schedule regardless of a specific trigger, simply because relying on someone noticing a trigger is not a reliable control on its own.

New hazard information
New data on a substance or mixture’s hazards becomes available that could affect the risk management measures already described.
Authorisation or restriction changes
An authorisation is granted or refused for a use covered by the SDS, or a new restriction is imposed that affects the substance or mixture.
A revised classification
The CLP classification changes, whether from new data, a harmonised classification, or a company’s own reassessment.
A specific request
Where risk management measures have been identified and a recipient asks for an update, or other legally defined triggers under Article 31(9) apply.
UK vs EU SAFETY DATA SHEETS

The same product, but not automatically the same document.

A single EU-format SDS is not automatically valid for the GB market, and vice versa, even where the underlying substance and classification are identical. Selling into both markets means maintaining both versions, and keeping each aligned with its own regime as UK REACH and EU REACH continue to develop on separate tracks.

UK / GB safety data sheets
Built to GB CLP classification and the UK REACH Annex II format, with supplier details for a GB-based entity and content in English. GB and EU requirements are largely aligned today, but each is free to diverge independently as the two regimes continue to develop separately.
EU safety data sheets
Built to EU CLP classification and the EU REACH Annex II format, supplied in the official language, or languages, of the Member State the product is placed in — which for a multi-market product can mean maintaining several language versions of the same underlying document.
HOW WE HELP

SDS that actually hold up to scrutiny.

An SDS sits downstream of classification, exposure assessment and use information, and it needs to stay accurate as all three continue to change.
We help organisations author new SDS to current REACH and CLP requirements, assess and prioritise fixes across existing SDS portfolios, and keep both GB and EU versions of a document aligned with their respective regimes as they diverge.
SDS authoring for new and reformulated products, to GB and EU requirements
Portfolio assessment and audit against current REACH and CLP requirements
Extended SDS (eSDS) and exposure scenario preparation
Update management as classifications, restrictions and authorisations change
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Product Stewardship Ltd provides specialist regulatory support, material assurance and compliance training for organisations operating across the UK, EU, industry and defence sectors.

Coverage: UK, EU & Defence sectors
Regulators: HSE & ECHA
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